BENZAMIDINE DERIVATIVES THEIR PREPARATION AND THEIR USE AS ANTI-COAGULANTS

Description

Field of the Invention

[0001] The present invention is directed to benzamidine derivatives and their pharmaceutically acceptable salts, which inhibit the enzyme, factor Xa, thereby being useful as anti-coagulants. It also relates to pharmaceutical compositions containing the derivatives or their pharmaceutically acceptable salts, and methods of their use.

BACKGROUND OF THE INVENTION

[0002] Factor Xa is a member of the trypsin-like serine protease dass of enzymes. A one-to-one binding of factors Xa and Va with calcium ions and phospholipid forms the prothrombinase complex which converts prothrombin to thrombin. Thrombin, in turn, converts fibrinogen to fibrin which polymerizes to form insoluble fibrin.

[0003] In the coagulation cascade, the prothrombinase complex is the convergent point of the intrinsic (surface activated) and extrinsic (vessel injury-tissue factor) pathways (Biochemistry (1991), Vol. 30, p. 10363; and Cell (1988), Vol. 53, pp. 505-518). The model of the coagulation cascade has been refined further with the discovery of the mode of action of tissue factor pathway inhibitor (TFPI) (Seminars in Hematology (1992), Vol. 29, pp. 159-161). TFPI is a circulating multi-domain serine protease inhibitor with three Kunitz-like domains which competes with factor Va for free factor Xa. Once formed, the binary complex of factor Xa and TFPI becomes a potent inhibitor of the factor VIIa and tissue factor complex.

[0004] Factor Xa can be activated by two distinct complexes, by tissue factor-VIIa complex on the "Xa burst" pathway and by the factor IXa-VIIIA complex (TENase) of the "sustained Xa" pathway in the coagulation cascade. After vessel injury, the "Xa burst" pathway is activated via tissue factor (TF). Up regulation of the coagulation cascade occurs via increased factor Xa production via the "sustained Xa" pathway. Down regulation of the coagulation cascade occurs with the formation of the factor Xa-TFPI complex, which not only removes factor Xa but also inhibits further factor formation via the "Xa burst" pathway. Therefore, the coagulation cascade is naturally regulated by factor Xa.

[0005] The primary advantage of inhibiting factor Xa over thrombin in order to prevent coagulation is the focal role of factor Xa versus the multiple functions of thrombin. Thrombin not only catalyzes the conversion of fibrinogen to fibrin, factor Vtll co VltIA, factor V to Va, and factor Xl to Xla, but also activates platelets, is a monocyte chemotactic factor, and mitogen for lymphocytes and smooth muscle cells. Thrombin activates protein C, the in vivo anti-coagulant inactivator of factors Va and Villa, when bound to thrombomodulin In circulation, thrombin is rapidly inactivated by antithrombin 111 (ATlll) and heparin cofactor if (HCII) in a reaction which is catalyzed by heparin or other proteolycan-associated glycosaminoglycans, whereas thrombin in tissues is inactivated by the protease, nexin. Thrombin carries out its multiple cellular activation functions through a unique "tethered ligand" thrombin receptor (Cell (1991), Vol. 64, p. 1057), which requires the same anionic binding site and active site used in fibrinogen binding and cleavage and by thrombomodulin binding and protein C activation. Thus, a diverse group of in vivo molecular targets compete to bind thrombin and the subsequent proteolytic events will have very different physiological consequences depending upon which cell type and which receptor, modulator, substrate or inhibitor binds thrombin.

[0006] Published data with the proteins antistasin and tick anti-coagulant peptide (TAP) demonstrate that factor Xa inhibitors are efficacious anti-coagulants (Thrombosis and Haemostasis (1992), Vol. 67, pp. 371-376; and Science (1990), Vol. 248, pp. 593-596).

[0007] The active site of factor Xa can be blocked by either a mechanism-based or a tight binding inhibitor (a tight binding inhibitor differs from a mechanism-based inhibitor by the lack of a covalent link between the enzyme and the inhibitor. Two types of mechanism-based inhibitors are known, reversible and irreversible, which are distinguished by ease of hydrolysis of the enzyme-inhibitor link (Thrombosis Res (1992), Vol. 67, pp. 221-231; and Trends Pharmacol. Sci. (1987), Vol. 8, pp. 303-307). A series of guanidino compounds are examples of tight-binding inhibitors (Thrombosis Res. (1980), Vol. 19, pp. 339-349). Arylsulfonyl-arginine-piperidinecarboxylic acid derivatives have also been shown to be tight-binding inhibitors of thrombin (Biochem. (1984), Vol. 23, pp. 85-90), as well as a series of arylamidine-containing compounds, including 3-amidinophenylaryl derivatives (Thrombosis Res. (1983), Vol. 29, pp. 635-642) and bis(amidino)benzyl cycloketones (Thrombosis Res. (1980), Vol. 17, pp. 545-548). However, these compounds demonstrate poor selectivity for factor Xa.

Related Disclosures

[0008] European Published Patent Application O 540 051 (Nagahara et al.) describes aromatic amidine derivatives which are stated to be capable of showing a strong anticoagulant effect through reversible inhibition of factor Xa.

[0009] The synthesis of α,α'-bis (amidinobenzylidene)cycloalkanones and α,α'-bis(amidinobenzyl)cycloalkanones is described in Pharmazie (1977), Vol. 32, No. 3, pp.141-145. These compounds are disclosed as being serine protease inhibitors.

[0010] GB-A- 824 908 discloses aromatic amidines containing a triacin moiety useful as antiparasitic agents.

[0011] Journal of the Chemical Society (1960), vol. 19, No. IV, pp. 4525-4532, deals with the synthesis of some amido anilino-1,3,5-triacines and their antiparasitic activity.

SUMMARY OF THE INVENTION

[0012] J. Med. Chem. (1976), vol. 19, No. 5, pp. 634-639, discloses aromatic bis (benzamidino) compounds as inhibitors of thrombin, kallicrein, and trypsin.

[0013] Thromb. Diath. haemorrh.(1975), Vol. 33, No. 2, pp 230-243, discloses aromatic bis(benzamidino) compounds as inhibitors of urokinase.

[0014] This invention is directed to compounds or their pharmaceutically acceptable salts which inhibit human factor Xa and are therefore useful as pharmacological agents for the treatment of disease-states characterized by thrombotic activity.

[0015] Accordingly, in one aspect, this invention provides compounds selected from the group consisting of the following formulae:







wherein

A

is -N =;

Z¹ and Z²

are independently -O-, -N(R⁸)-, -S-, or -OCH₂-;

R¹ and R³

are independently hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, -N(R⁸)⁹R, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹², or -N(R⁸)C(O)N(R⁸)CH₂C(O)N(R⁸R⁹;

R²

is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; _-C(O)N(R⁸)R⁹; -N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_m,C(O)OR⁸ (where m is 0 to 3); -NCR⁸) (CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O (CH₂)_pC(O)OR⁸ (where p is 1 to 6); N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²

is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo; alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, amino_carbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²

is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R8)R9, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, and tetrazolylalkyi);

or R²

is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the " piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonylalkyi and aralklyl);

or R²

is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴ and R⁷

are independently hydrogen, halo, alkyl, nitro, -OR⁸, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -N(H)C(O)R⁸, or -N(H)S(O)₂R¹²;

R⁵

is -C(NH)NH₂, -C(NH)N(H)OR⁸, -C(NH)N(H)C(O)OR¹², -C(NH)N(H)S(O)₂R¹²_, -C(NH)N(H)C(O)N(R⁸)R⁹, or -C(NH)N(H)C(O)R⁸;

R⁶

is halo, alkyl, haloalkyl, haloalkoxy, nitro, amino, ureido, guanidino, -OR⁸, -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH₂)_mC(O)N(R⁸)R⁹ (where m is O to 3), -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), -(CH₂)_mC(O)OR⁸ (where m is 0 to 3), -N(H)C(O)R⁸, (1,2)-tetrahydropyrimidinyl (optionally substituted by alkyl), (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl);

each R⁸ and R⁹

is independently hydrogen, alkyl, aryl, or aralkyl;

R¹⁰

is hydrogen, alkyl, aryl, aralkyl, 1-pyrrolidinyl, 4-morpolinyl, 4-piperazinyl, 4-(N-methyl)piperazinyl, or piperidin-1-yl;

R¹¹

is hydrogen, alkyl or halo; and

R¹²

is alkyl, aryl or aralkyl;

or a pharmaceutically acceptable salt thereof.

[0016] In another aspect, this invention provides compositions useful in treating a human having a disease-state characterized by thrombotic activity, which composition comprises a therapeutically effective amount of a compound of the invention as described above, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

[0017] In another aspect, this invention provides a method of treating a human having a disease-state characterized by thrombotic activity, which method comprises administering to a human in need thereof a therapeutically effective amount of a compound of the invention as described above.

[0018] In another aspect, this invention provides a method of treating a human having a disease-state alleviated by the inhibition of factor Xa, which method comprises administering to a human in need thereof a therapeutically effective amount of a compound of the invention as described above.

[0019] In another aspect, this invention provides a method of inhibiting human factor Xa in vitro or in vivo by the administration of a compound of the invention.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

[0020] As used in the specification and appended claims, unless specified to the contrary, the following terms have the meaning indicated:

"Halo" refers to bromo, chloro or fluoro.

"Aminocarbonyl" refers to the radical -C(O)NH₂.

"Amidino" refers to the radical -C(NH)NH₂.

"Benzamidine" refers to a phenyl radical substituted by an amidino radical.

"Carboxy" refers to the radical -C(O)OH.

"Dimethylaminocarbonyl" refers to the radical -C(O)N(CH₃)₂.

"Alkyl" refers to a straight or branched chain monovalent or divalent radical consisting solely of carbon and hydrogen, containing no unsaturation and having from one to six carbon atoms, e.g., methyl, ethyl, n-propyl, 1-methylethyl (iso-propyl), n-butyl, n-pentyl, 1,1-dimethylethyl (t-butyl), and the like.

"Alkenyl" refers to a straight or branched chain monovalent or divalent radical consisting solely of carbon and hydrogen, containing at least one double bond and having from one to six carbon atoms, e.g., ethenyl, prop-1-enyl, but-1-enyl, pent-1-enyl, pent-1,4-dienyl, and the like.

"Haloalkyl" refers to an alkyl radical, as defined above, that is substituted by one or more halo radicals, as defined above, e.g., trifluoromethyl; difluoromethyl, trichloromethyl, 2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl, 3-bromo-2-fluoropropyl, 1-bromomethyl-2-bromoethyl, and the like.

"Haloalkoxy" refers to a radical of the formula -OR_b wherein R_b is haloalkyl as defined above, e.g., trifluoromethoxy, difluoromethoxy, trichloromethoxy, 2-trifluoroethoxy, 1-fluoromethyl-2-fluoroethoxy, 3-bromo-2-fluoropropoxy, 1-bromomethyl-2-bromoethoxy, and the like.

"Aryl" refers to a phenyl or naphthyl radical optionally substituted by halo, alkyl, alkoxy, amino, nitro or carboxy.

"Aralkyl" refers to a radical of the formula -R_aR_c where R_a is alkyl as defined above and R_c is aryl as defined above, e.g., benzyl.

"Aryloxy" refers to a radical of the formula -OR_c where R_c is phenyl or naphthyl, e.g., phenoxy and naphthoxy.

"Alkoxy" refers to a radical of the formula -OR_a where R_a is alkyl as defined above, e.g., methoxy, ethoxy, n-propoxy, 1-methylethoxy (iso-propoxy), n-butoxy, n-pentoxy, 1,1-dimethylethoxy (t-butoxy), and the like.

"Alkanol" refers to a branched or unbranched aliphatic hydrocarbon of 1 to 6 carbons wherein one hydroxyl radical is attached thereto, e.g., methanol, "thanol, isopropanol, and the like.

"Aminocarbonylalkyl" refers to a radical of the formula -R_aC(O)NH₂ wherein R_a is alkyl as defined above, e.g., aminocarbonylmethyl, 2-aminocarbonylethyl, 3-aminocarbonylpropyl, 1,1-dimethyl-2-aminocarbonylethyl, and the like.

"(Alkylamino)carbonylalkyl" refers to a radical of the formula -R_aC(O)N(H)R_a wherein each R_a is the same or different and is alkyl as defined above, e.g., (methylamino)carbonylmethyl 1, 2-(ethylamino)carbonylethyl, 3-(methylamino)-carbonylpropyl, 1,1-dimethyl-2-(ethylamino)carbonylethyl, and the like.

"(Dialkylamino)carbonylalkyl" refers to a radical of the formula -R_aC(O)N(R_a)₂ wherein each R_a is the same or different and is alkyl as defined above, e.g., (dimethyl)amino)carbonylmethyl, 2-(diethylamino)carbonylethyl, 3-(dimethylamino)carbonylpropyl, 1,1-dimethyl-2-(diethylamino)carbonylethyl, and the like.

"(Arylamino)carbonylalkyl" refers to a radical of the formula -R_aC(O)N(H)R_c wherein R_a is alkyl as defined above and R_c is aryl as defined above, e.g., phenylaminocarbonylmethyl, 2-phenylaminocarbonylethyl, 3-phenylaminocarbonylpropyl, 1,1-dimethyl-2-phenylaminocarbonylethyl, and the like.

"(Aralkylamino)carbonylalkyl" refers to a radical of the formula R_aC(O)N(H)R_c wherein R_a is alkyl as defined above and R_d is aralkyl as defined above, e.g., benzylaminocarbonylmethyl, 2-benzylaminocarbonylethyl,3-benzylaminocarbonylpropyl, 1, 1-dimethyl-2-benzylaminocarbonylethyl, and the like.

"Alkoxycarbonylalkenyl" refers to a radical of the formula R_eC(O)OR_a wherein R_a is lower alkyl as defined above and R_e is alkenyl as defined above, e.g., 2-methoxycarbonylethenyl, 3-methoxycarbonyprop-1-enyl, 2-ethoxycarbonylethenyl, and the like.

"Carboxyalkenyl" refers to a radical of the formula -R_eC(O)OH where R_e is alkenyl as defined above, e.g., 2-carboxyethenyl, 3-carboxyprop-1-enyl, 4-carboxybut-1-enyl, and the like.

"Aminocarbonylalkenyl" refers to a radical of the formula -R_eC(O)NH₂ wherein R_e is alkenyl as defined above, e.g., 2-aminocarbonylethenyl, 3-aminocarbonylprop-1-enyl, 1-methyl-2-aminocarbonylethenyl, and the like.

"(Alkylamino)carbonylalkenyt" refers to a radical of the formula -R_eC(O)N(H)R_a wherein R_a is alkyl as defined above and R_e is alkenyl as defined above, e.g., 2-(ethylamino)carbonylethenyl, 3-(methylamino)carbonylprop-1-enyl, 1-methyl-2-(ethylamino)carbonylethenyl, and the like.

"(Dialkylamino)carbonylalkenyl" refers to a radical of the formula R_eC(O)N(R_a)₂ wherein each R_a is the same or different and is as defined above and R_e is alkenyl as defined above, e.g., 2-(diethylamino)carbonylethenyl, 3-(dimethylamino)carbonylprop-1-enyl, 1-methyl-2-(diethylamino)carbonylethenyl, and the like.

"(Arylamino)carbonylalkenyl" refers to a radical of the formula R_eC(O)N(H)R_c wherein R_c is aryl as defined above and R_e is alkenyl as defined above, e.g., 2-(phenylamino)carbonylethenyl, 3-(phenylamino)carbonylprop-1-enyl, 1-methyl-2-(phenylamino)carbonylethenyl, and the like.

"(Aralkylamino)carbonylalkenyl" refers to a radical of the formula R_eC(O)N(H)R_d wherein R_d is aralkyl as defined above and R_e is alkenyl as defined above, e.g., 2-(benzylamino)carbonylethenyl, 3-(benzylamino)carbonylprop-1-enyl, 1-methyl-2-(benzylamino)carbonylethenyl, and the like.

"(Hydroxyalkoxy)carbonyl" refers to a radical of the formula -C(O)OR_a wherein R_a is alkyl as defined above substituted by a hydroxy radical, e.g., 2-(hydroxy)ethoxycarbonyl, 3-(hydroxy)propoxycarbonyl, 5-(hydroxy)pentoxycarbonyl, and the like.

"(Alkoxy)alkoxycarbonyl" refers to a radical of the formula -C(O)OR_aOR_a wherein each R_a is the same or different and is alkyl as defined above, e.g., 2-(methoxy)ethoxycarbonyl, 3-(methoxy)propoxycarbonyl, 5-(ethoxy)pentoxycarbonyl, and the like.

"(Hydroxyalkoxy)alkoxycarbonyl" refers to a radical of the formula -C(O)OR_aOR_a, wherein each R_a is the same or different and is alkyl as defined above, and the terminal R_a radical is substituted by a hydroxy radical, e.g., 2-(2-hydroxyethoxy)ethoxycarbonyl, 2-(3-hydroxypropoxy)ethoxycarbonyl, and the like.

"((Alkoxy)alkoxy)alkoxycarbonyl" refers to a radical of the formula -C(O)OR_aOR_aOR_a where each R_a is the same or different and is alkyl as defined above, e.g., 2-(2-(methoxy)ethoxy)ethoxycarbonyl, 3-(2-(methoxy)ethoxy)propoxycarbonyl, 4-(3-ethoxy)propoxy]butoxycarbonyl, and the like.

"Haloalkoxycarbonyl" refers to a radical of the formula -C(O)OR_b wherein R_b is haloalkyl as defined above, e.g., trifluoromethoxycarbonyl, difluoromethoxycarbonyl, trichloromethoxycarbonyl, 2-trifluoroethoxycarbonyl,1-fluoromethyl-2-fluoro-ethoxycarbonyl,3-bromo-2-fluoropropoxycarbonyl, 1-bromomethyl-2-bromoethoxy-carbonyl, and the like.

"Carboxyalkyl" refers to a radical of the formula -R_aC(O)OH where R_a is alkyl as defined above, e.g., carboxymethyl, 2-carboxyethyl, 3-carboxypropyl, and the like.

"Alkoxycarbonyl" refers to a radical of the formula -C(O)OR_a wherein R_a is alkyl as defined above, e.g., methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, and the like.

"Alkoxycarbonylalkyl" refers to a radical of the formula -R_aC(O)OR_a wherein each R_a is the same or different and is alkyl as defined above, e.g., methoxycarbonylethyl, ethoxycarbonylethyl, '-butoxycarbonylethyl, and the like.

"Morpholin-4-ylalkyl" refers to a radical of the formula -R_aR_f where R_a is alkyl as defined above and R_f is a morpholin-4-yl radical, e.g., morpholin-4-ylmethyl, morpholin-4-ylethyl, and the like.

"4-morpholinoyl" refers to a radical of the formula -C(0)R_f where R_f is a morpholin-4-yl radical.

"(3,4)-Piperidinyloxy" refers to a radical of the formula -OR_g where R_g is a piperidinyl radical attached to the oxygen atom at either the 3- or 4-position.

"3-Tetrahydrofuranyloxy" refers to the radical of the formula -OR_h where R_h is a tetrahydrofuranyl radical attached to the oxygen atom at the 3-position.

"3-Pyrrolidinyloxy" refers to the radical of the formula -OR_i where R_i is a pyrrolidinyl radical attached to the oxygen atom at the 3-position.

"1-Piperazinoyl" refers to the radical of the formula -C(O)R_j where R_j is piperazin-1-yl.

"1-Piperidinoyl" refers to the radical of the formula -C(O)R_k where R_k is piperidin-1-yl.

"1-Pyrrolidinoyl" refers to the radical of the formula -C(O)R_m where R_m is pyrrolidin-1-yl.

"(1,2)-Imidazolyl" refers to an imidazolyl radical attached at either the 1- or 2-position.

"(1,2)-Imidazolinyl" refers to a 4,5-dihydroimidazolyl radical attached at either the 1- or the 2-position.

"DMSO" refers to dimethyl sulfoxide.

"HPLC" refers to high performance liquid chromatography.

"Optional" or "optionally" means that the subsequently described event of circumstances may or may not occur, and that the description includes instances where said event or circumstance occurs and instances in which it does not. For example, "optionally substituted aryl" means that the aryl radical may or may not be substituted and that the description includes both substituted aryl radicals and aryl radicals having no substitution.

"Pharmaceutically acceptable salt" includes both acid and base addition salts.

"Pharmaceutically acceptable acid addition salt" refers to those salts which retain the biological effectiveness and properties of the free bases, which are not biologically or otherwise undesirable, and which are formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like, and organic acids such as acetic acid, trifluoroacetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, and the like.

"Pharmaceutically acceptable base addition salt" refers to those salts which retain the biological effectiveness and properties of the free acids, which are not biologically or otherwise undesirable. These salts are prepared from addition of an inorganic base or an organic base to the tree acid. Salts derived from inorganic bases include, but are not limited to, the sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum salts and the like. Preferred inorganic salts are the ammonium, sodium, potassium, calcium, and magnesium salts. Salts derived from organic bases include, but are not limited to, salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-dimethylaminoethanol, 2-diethylaminoethanol, trimethamine, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, polyamine resins and the like. Particularly preferred organic bases are isopropylamine, diethylamine, ethanolamine, trimethamine, dicyclohexylamine, choline and caffeine.

"Therapeutically effective amount" refers to that amount of a compound of formula (I) which, when administered to a human in need thereof, is sufficient to effect treatment, as defined below, for disease-states characterized by thrombotic activity. The amount of a compound of formula (I) which constitutes a "therapeutically effective amount" will vary depending on the compound, the disease-state and its severity, and the age of the human to be treated, but can be determined routinely by one of ordinary skill in the art having regard to his own knowledge and to this disclosure.

"Treating" or "treatment" as used herein cover the treatment of a disease-state in a human, which disease-state is characterized by thrombotic activity; and include:

(i) preventing the disease-state from occurring in a human, in particular, when such human is predisposed to the disease-state but has not yet been diagnosed as having it;

(ii) inhibiting the disease-state, i.e., arresting its development; or

(iii) relieving the disease-state, i.e., causing regression of the disease-state.

[0021] The yield of each of the reactions described herein is expressed as a percentage of the theoretical yield.

[0022] The compounds of the invention, or their pharmaceutically acceptable salts, may have asymmetric carbon atoms in their structure. The compounds of the invention and their pharmaceutically acceptable salts may therefore exist as single stereoisomers, racemates, and as mixtures of enantiomers and diastereomers. All such single stereoisomers, racemates and mixtures thereof are intended to be within the scope of this invention.

[0023] The nomenclature used herein is a modified form of the I.U.P.A.C. system wherein the compounds of the invention are named as derivatives of benzamidine. For example, a compound of the invention selected from formula (I), i.e.,

   wherein A is -N=, Z¹ and Z² are both -O-, R¹ and R³ are both fluoro, R² is methyl, R⁴ is methoxy, R⁵ is -C(NH)NH₂, R⁶ is dimethylamino, and R⁷ is hydrogen, that is, a compound of the following formula:

is named herein as 4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine.

Utility and Administration

A. Utility

[0024] The compounds of the invention are inhibitors of factor Xa and therefore useful in disease-states characterized by thrombotic activity based on factor Xa's role in the coagulation cascade (see Background of the Invention above). A primary indication for the compounds is prophylaxis for long term risk following myocardial infarction. Additional indications are prophylaxis of deep vein thrombosis (DVT) following orthopedic surgery or prophylaxis of selected patients following a transient ischemic attack. The compounds of the invention may also be useful for indications in which coumadin is currently used, such as for DVT or other types of surgical intervention such as coronary artery bypass graft and percutaneous transluminal coronary angioplasty. The compounds are also useful for the treatment of thrombotic complications associated with acute promyelocytic leukemia, diabetes, multiple myelomas, disseminated intravascular coagulation associated with septic shock, purpura fulminanas associated infection, adult respiratory distress syndrome, unstable angina, and thrombotic complications associated with aortic valve or vascular prosthesis. The compounds are also useful for prophylaxis for thrombotic diseases, in particular in patients who have a high risk of developing such disease.

[0025] In addition, the compounds of the invention are useful as in vitro diagnostic reagents for selectively inhibiting factor Xa without inhibiting other components of the coagulation cascade.

B. Testing

[0026] The primary bioassays used to demonstrate the inhibitory effect of the compounds of the invention on factor Xa are simple chromogenic assays involving only serine protease, the compound of the invention to be tested, substrate and buffer (see, e.g., Thrombosis Res. (1979), Vol. 16, pp. 245-254). For example, four tissue human serine proteases can be used in the primary bioassay, free factor Xa, prothrombinase, thrombin (lla) and tissue plasminogen activator (tPA). The assay for tPA has been successfully used before to demonstrate undesired side effects in the inhibition of the fibrinolytic process (see, e.g., J. Med. Chem. (1993), Vol. 36, pp. 314-319). Another bioassay useful in demonstrating the utility of the compounds of the invention in inhibiting factor Xa demonstrates the potency of the compounds against free factor Xa in citrated plasma. For example, the anticoagulant efficacy of the compounds of the invention will be tested using either the prothrombin time (PT), or activated partial thromboplastin time (aPTT) while selectivity of the compounds is checked with the thrombin clotting time (TCT) assay. Correlation of the K_i in the primary enzyme assay with the K_i for free factor Xa in citrated plasma will screen against compounds which interact with or are inactivated by other plasma components. Correlation of the K_i with the extension of the PT is a necessary in vitro demonstration that potency in the free factor Xa inhibition assay translates into potency in a clinical coagulation assay. In addition, extension of the PT in citrated plasma can be used to measure duration of action in subsequent pharmacodynamic studies.

[0027] For further information on assays to demonstrate the activity of the compounds of the invention, see R. Lottenberg et al., Methods in Enzymology (1981), Vol. 80, pp. 341-361, and H. Ohno et al., Thrombosis Research (1980), Vol. 19, pp. 579-588.

C. General Administration

[0028] Administration of the compounds of the invention, or their pharmaceutically acceptable salts, in pure form or in an appropriate pharmaceutical composition, can be carried out via any of the accepted modes of administration or agents for serving similar utilities. Thus, administration can be, for example, orally, nasally, parenterally, topically, transdermally, or rectally, in the form of solid, semi-solid, lyophilized powder, or liquid dosage forms, such as for example, tablets, suppositories, pills, soft elastic and hard gelatin capsules, powders, solutions, suspensions, or aerosols, or the like, preferably in unit dosage forms suitable for simple administration of precise dosages. The compositions will include a conventional pharmaceutical carrier or excipient and a compound of the invention as the/an active agent, and, in addition, may include other medicinal agents, pharmaceutical agents, carriers, adjuvants, etc.

[0029] Generally, depending on the intended mode of administration, the pharmaceutically acceptable compositions will contain about 1 % to about 99% by weight of a compound(s) of the invention, or a pharmaceutically acceptable salt thereof, and 99% to 1 % by weight of a suitable pharmaceutical excipient. Preferably, the composition will be about 5% to 75% by weight of a compound(s) of the invention, or a pharmaceutically acceptable salt thereof, with the rest being suitable pharmaceutical excipients.

[0030] The preferred route of administration is oral, using a convenient daily dosage regimen which can be adjusted according to the degree of severity of the disease-state to be treated. For such oral administration, a pharmaceutically acceptable composition containing a compound(s) of the invention, or a pharmaceutically acceptable salt thereof, is formed by the incorporation of any of the normally 4 employed excipients, such as, for example, pharmaceutical grades of mannitol, lactose, starch, pregelatinized starch, magnesium stearate, sodium saccharine, talcum, cellulose ether derivatives, glucose, gelatin, sucrose, citrate, propyl gallate, and the like. Such compositions take the form of solutions, suspensions, tablets, pills, capsules, powders, sustained release formulations and the like.

[0031] Preferably such compositions will take the form of capsule, caplet or tablet and therefore will also contain a diluent such as lactose, sucrose, dicalcium phosphate, and the like; a disintegrant such as croscarmellose sodium or derivatives thereof; a lubricant such as magnesium stearate and the like; and a binder such as a starch, gum acacia, polyvinylpyrrolidone, gelatin, cellulose ether derivatives, and the like.

[0032] The compounds of the invention, or their pharmaceutically acceptable salts, may also be formulated into a suppository using, for example, about 0.5% to about 50% active ingredient disposed in a carrier that slowly dissolves within the body, e.g., polyoxyethylene glycols and polyethylene glycols (PEG), e.g., PEG 1000 (96%) and PEG 4000 (4%).

[0033] Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing, etc., a compound(s) of the invention (about 0.5% to about 20%), or a pharmaceutically acceptable salt thereof, and optional pharmaceutical adjuvants in a carrier, such as, for example, water, saline, aqueous dextrose, glycerol, ethanol and the like, to thereby form a solution or suspension.

[0034] If desired, a pharmaceutical composition of the invention may also contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, antioxidants, and the like, such as, for example, citric acid, sorbitan monolaurate, triethanolamine oleate, butylated hydroxytoluene, etc.

[0035] Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, 18th Ed., (Mack Publishing Company, Easton, Pennsylvania, 1990). The composition to be administered will, in any event, contain a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, for treatment of a disease-state alleviated by the inhibition of factor Xa in accordance with the teachings of this invention.

[0036] The compounds of the invention, or their pharmaceutically acceptable salts, are administered in a therapeutically effective amount which will vary depending upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of the compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular disease-states, and the host undergoing therapy. Generally, a therapeutically effective daily dose is from about 0.14 mg to about 14.3 mg/kg of body weight per day of a compound of the invention, or a pharmaceutically acceptable salt thereof; preferably, from about 0.7 mg to about 10 mg/kg of body weight per day; and most preferably, from about 1.4 mg to about 7.2 mg/kg of body weight per day. For example, for administration to a 70 kg person, the dosage range would be from about 10 mg to about 1.0 gram per day of a compound of the invention, or a pharmaceutically acceptable salt thereof, preferably from about 50 mg to about 700 mg per day, and most preferably from about 100 mg to about 500 mg per day.

Preferred Embodiments

[0037] Of the compounds of the invention as set forth above in the Summary of the Invention, several groups of compounds are preferred.

[0038] One preferred group are those compounds selected from formula (I):

wherein

A

is -N=;

Z¹ and Z²

are independently -O-, -N(R⁸)- or -OCH₂-;

R¹ and R³

are independently hydrogen, fluoro, chloro, haloalkyl, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, or -N(R⁸)S(O)₂R¹²;

R²

is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -C(O)N(R⁸)R⁹; N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3); -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²

is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, ami_nocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, aminocarbonylalkenyl, (alkytamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl);

or R²

is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, or alkoxycarbonylalkyl);

or R²

is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, or tetrazolylalkyl);

or R²

is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonylalkyl or aralklyl);

or R²

is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl, -C(O)N(R⁸)R⁹, or alkoxycarbonylalkyl);

R⁴

is hydrogen, -OR⁸ or -N(R⁸)R⁹;

R⁵

is-C(NH)NH₂;

R⁶

is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), 1-piperidinoyl, 1-pyrrolidinoy), (1 ,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl);

R⁷

is hydrogen, halo, alkyl, -OR⁸, -C(O)N(R⁸)R⁹;

R⁸ and R⁹

are independently hydrogen, methyl, ethyl or phenyl; and

R¹²

is methyl, ethyl, phenyl or benzyl. Of this group of compounds, a preferred subgroup of compounds is that subgroup wherein

Z¹ and Z²

are independently -O- or -NCH₃-;

R¹ and R³

are independently hydrogen, fluoro, chloro, trifluoromethyl, amino, -C(O)N(R⁸)R⁹, or -NHC(O)NHR⁹;

R²

is hydrogen; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -N(R⁸)R⁹; -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²

is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, alkoxycarbonylalkyi, carboxyalkyi, alkoxycarbonylalkenyl, carboxyalkenyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²

is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxyalkyl, and alkoxycarbonylalkyl);

or R²

is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy and alkoxycarbonyl);

or R²

is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl and alkoxycarbonylalkyl);

or R²

is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl, alkoxycarbonylalkyl and aralklyl);

or R²

is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴

is hydrogen, amino, hydroxy, or methoxy;

R⁵

is -C(NH)NH₂;

R⁶

is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 to 1), (1,2)-imidazolyl substituted by alkyl, or 2-imidazolinyl substituted by alkyl;

R⁷

is hydrogen, methoxy, or hydroxy; and

R⁸ and R⁹

are independently hydrogen, methyl, ethyl, or phenyl.

[0039] Of this subgroup of compounds, a preferred class of compounds is that class wherein Z¹ and Z² are both -O-; R¹ and R³ are independently hydrogen, fluoro, or chloro; R⁴ is amino, hydrogen, hydroxy or methoxy; R⁶ is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 or 1), (1,2)-imidazolyl substituted by methyl, or 2-imidazolinyl optionally substituted by methyl; and R⁷ is hydrogen or hydroxy.

[0040] Of this class of compounds, a preferred subclass of compounds is that subclass wherein R⁴ is hydroxy; R⁶ is dimethylamino or dimethylaminocarbonyl; and R⁷ is hydrogen.

[0041] Of this subclass of compounds, preferred compounds are selected from the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonyl-methylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4 hdroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1, 3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-bromo-3-fluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((methyl)-(carboxymethyl)arnino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(piperidin-1-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-13-dimethyiaminocarbonylphenoxy)-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(morpholin-4-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxymethylpiperazinyl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonylmethylpiperazinyl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-(morpholin-4-ylmethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-carboxymethoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl]oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-carboxymethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-((carboxymethyl)aminocarbonylmethyl)amino]pyridin-2-yl)oxy]benzamidine.

[0042] Of this class of compounds, another preferred subclass of compounds is that subclass wherein wherein R⁴ is hydroxy; R⁶ is (1,2)-imidazolyl substituted by methyl or 2-imidazolinyl substituted by methyl; and R⁷ is hydrogen.

[0043] Of this subclass, preferred compounds are selected from the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)-(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-(1-(methoxycarbonyl)ethyl)piperidin-4-yl)aminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-[1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-dlfluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-ditluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(-3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)4-(3-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2yl)oxy]benzamidine.

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-4-(3-(1-methylimidazolin-2-yl)phenoxy)-6-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chloro-4-carboxyphenoxy) pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethyl)piperidin-4-yloxy)pyridin-2yl)oxy]benzamidine;

4-hydroxy-3-[(3 ,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(ethoxycarbonylmethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difiuoro-6-(3-(1-melhylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxy-carbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-(ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy(-4-((piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypent-1-oxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine.

[0044] Of this class of compound, another preferred subclass of compounds is that subclass where R⁴ is hydroxy; R⁶ is guanidino; and R⁷ is hydrogen.

[0045] Of this subclass of compounds, preferred compounds are selected from the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-ethoxycarbonylmethyl)-piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-guanidino)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(methyl)(phenyl)aminocarbonylpyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine.

[0046] Another preferred group of compounds are selected from formula (VII):

wherein

Z¹ and Z²

are independently -O-, -N(R⁸)- or -OCH₂-;

R¹ and R³

are independently hydrogen, fluoro, chloro, haloalkyl, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, or -N(R⁸)S(O)₂P¹²;

R²

is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -C(O)N(R⁸)R⁹; - N(R⁸)R⁹; C(O)N(R⁸)(CH₂)_m(CO)OR⁸ (where m is 0 to 3); -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²

is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylafkyl, alkoxycarbonylalkenyl, carboxy_alkenyl. aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²

is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²

is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, or alkoxycarbonylalkyl);

or R²

is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, or tetrazolylalkyl);

or R²

is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonylalkyl or aralklyl);

or R²

is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonyl or alkoxycarbonylalkyl);

R⁴

is hydrogen, -OR⁸ or -N(R⁸)R⁹:

R⁵

is -C(NH)NH₂;

R⁶

is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), 1-piperidinoyl, 1-pyrrolidinoyl, (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl);

R⁷

is hydrogen, halo, alkyl, -OR⁸, -C(CO)N(R⁸)R⁹;

R⁸ and R⁹

are independently hydrogen, methyl, ethyl or phenyl;

R¹²

is methyl, ethyl, phenyl or benzyl.

[0047] Of this group of compounds, a preferred subgroup of compounds is that subgroup wherein

Z¹ and Z²

are independently -O- or -NCH₃-;

R¹ and R³

are independently hydrogen, fluoro, chloro, trifluoromethyl, amino, -C(O)N(R⁸)R⁹, or -NHC(O)NHR⁹;

R²

is hydrogen; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -N(R⁸)R⁹; -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); N(R⁸)(CH_2)nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²

is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²

is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxyalkyl, and alkoxycarbonylalkyl);

or R²

is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy and alkoxycarbonyl);

or R²

is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl and alkoxycarbonylalkyl);

or R²

is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl, alkoxycarbonylalkyl and aralklyl);

or R²

is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴ is

hydrogen, amino, hydroxy, or methoxy;

R⁵ is

-C(NH)NH₂;

R⁶ is

guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 to 1), (1,2)-imidazolyl substituted by alkyl, or 2-imidazolinyl substituted by alkyl;

R⁷ is

hydrogen, methoxy, or hydroxy; and

R⁸ and

R⁹ are independently hydrogen, methyl, ethyl, or phenyl.

[0048] Of this subgroup of compounds, a preferred class of compounds is that class wherein Z¹ and Z² are both -O-; R¹ and R³ are independently hydrogen, fluoro, or chloro; R⁴ is amino, hydrogen, hydroxy or methoxy; R⁶ is guanidino, -C(NH)NH₂. -C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 or 1), (1,2)-imidazolyl substituted by methyl, or 2-imidazolinyl optionally substituted by methyl; and R⁷ is hydrogen or hydroxy. .

[0049] Of this class of compounds, a preferred subclass of compounds is that subclass wherein R⁴ is hydroxy; R⁶ is dimethylamino or dimethylaminocarbonyl; and R⁷ is hydrogen.

[0050] Of this subclass of compounds, preferred compounds are 4-hydroxy-3-[(3,5-difluoro-6 and
4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonyl-phenoxy)-2-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-4-yl)oxy]benzamidine.

Preparation of Compounds of The Invention

[0051] As a matter of convenience, the following description of the preparation of the compounds of the invention is directed to the preparation of compounds of formula (I). It is understood, however, that similar synthetic processes may be used to prepare the compounds of formula (II), (III), (IV), (V), (VI), (VII) and (VIII). It is also understood that in the following description, combinations of substituents and/or variables (e.g., R⁴ and R⁵) on the depicted formulae are permissible only if such combinations result in stable compounds.

A. Preparation of Intermediates

1. Compounds of formula (C)

[0052] Compounds of formula (C), as shown below, are intermediates in the preparation of the compounds of the invention. As illustrated below in Reaction Scheme 1, compounds of formula (C) are prepared from compounds of formulae (A) and (B) wherein X is chloro or fluoro and R^2a is -N(R⁸)R⁹, -N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3) or piperazinyl (optionally substituted by alkyl, carboxy, carboxyalkyl, alkoxycarbonyl or alkoxycarbonylalkyl); and each R⁸ and R⁹ is independently hydrogen, alkyl, aryl or aralkyl:

[0053] Compounds of formula (A) and (B) can be prepared according to methods known to those of ordinary skill in the art or are commercially available, for example, from Aldrich Chemical Company, Inc. or from Maybridge Co.

[0054] In general, compounds of formula (C) are prepared by reacting a compound of formula (A) with an equimolar amount of a compound of formula (B) at 0°C to 40°C, preferably at ambient temperature, in the presence of a base, e.g., triethylamine, or in the presence of a second equivalent of the compounds of formula (B). The compounds of formula (C) are isolated from the resulting reaction mixture by conventional methods.

2. Compounds of formula (F)

[0055] Compounds of formula (F), as shown below, are also intermediates in the preparation of the compounds of the invention. As illustrated below in Reaction Scheme 2, compounds of formula (F) are prepared from compounds of formulae (D) and (E) where each X is independently chloro or fluoro; and R² is alkoxy, haloalkoxy, -O(CH)_pC(O)OR⁸ (where p is 1 to 6), -N(R⁸)R⁹, -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3), morpholin-4-yl, 3-tetrahydrofuranyloxy; or R² is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, larylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxylalkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl)); or R² is 1-piperidinyl (optionally substituted by alkoxycarbonyl or alkoxycarbonylalkyl); or R² is 1-piperazinyl (optionally substituted by alkyl, alkoxycarbonyl or alkoxycarbonylalkyi); or R² is (3,4)-piperidinyloxy (optionally substituted by alkylcarbonyl, alkoxycarbonyl, alkoxycarbonylalkyl or tetrazolylalkyl); or R² is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by alkyl, alkoxycarbonyl, alkoxycarbonylalkyl or aralklyl); or R² is 3-pyrrolidinyloxy (optionally substituted by alkyl, aralkyl or alkoxycarbonylalkyl); and each R⁸ and R⁹ is independently hydrogen, alkyl, aryl or aralkyl:

[0056] Compounds of formulae (D) and (E) are commercially available, for example, from Aldrich Chemical Company, Inc., or may be prepared according to methods known to those skilled in the art.

[0057] In general, compounds of formula (F) are prepared by treating a compound of formula (D) with a compound of formula (E) in an aprotic solvent, for example, methylene chloride, at between about 0°C and 50°C, preferably at ambient temperature, and, if the hydrogen in the compound of formula (E) is an hydroxyl hydrogen, in the presence of a base, for example, cesium carbonate. The compound of formula (F) is isolated from the reaction mixture by standard techniques.

3. Compounds of formulae (J) and (K)

[0058] Compounds of formulae (J) and (K), as shown below, are also intermediates in the preparation of the compounds of the invention. As illustrated below in Reaction Scheme 3, compounds of formula (J) and (K) are prepared from compounds of formula (G) and formula (H) where A is -N= or -C(R¹¹)= (where R¹¹ is hydrogen, alkyl or halo); X is fluoro of chloro; R¹ and R³ are independently hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹², or -N(R⁸)C(O)N(R⁸)CH₂-C(O)N(R⁸)R⁹; R² is hydrogen, alkyl, haloalkoxy, -OR¹², -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3), -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3), -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3), -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3), -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3), morpholin-4-yl, 3-tetrahydrofuranoxy; or R² is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR¹², -C(O)N(R⁸)R⁹, halo, alkyl, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl)); or R² is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, alkoxycarbonyl, alkoxycarbonylalkyl, and tetrazolylalkyl); or R² is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, alkoxycarbonylalkyl and aralklyl); or R² is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, alkoxycarbonyl and alkoxycarbonylalkyl); R⁴ is independently hydrogen, halo, alkyl, nitro, -OR¹², -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, or -N(H)C(O)R⁸; each R⁸ and R⁹ is independently hydrogen, alkyl, aryl or aralkyl; and R¹² is alkyl, aryl or aralkyl:

[0059] Compounds of formula (G) include comp unds of formulae (C) and (F) as described above, or may be prepared by methods described herein or by methods known to one of ordinary skill in the art. They may also be commercially available, for example, from Aldrich Chemical Co., Inc. or from Maybridge Co. Compounds of formula (H) may be prepared by methods known to one of ordinary skill in the art or may be commercially available, for example, from Aldrich Chemical Co., Inc.

[0060] In general, the compounds of formulae (J) and (K) are prepared by reacting a compound of formula (G) with a compound of formula (H) (in an equimolar amount for a compound of formula (K) and with two or more equivalents of a compound of formula (H) for a compound of formula (J)) in the presence of a base, e.g., sodium hydride or cesium carbonate, at temperatures between about 20°C and 120°C, preferably, for compounds of formula (J), at temperatures of around 50°C, in an aprotic solvent, for example, dimethylformamide, DMSO or acetonitrile, for a period of time sufficient to complete the desired reaction as monitored by thin layer chromatography (TLC). Compounds of formulae (J) and (K) are then isolated from the reaction mixture by standard isolation techniques.

[0061] In a similar manner, compounds of formula (G) may be treated with compounds of formula (H) wherein the hydroxy group is replaced by an amino group to produce compounds of formulae (J) and (K) wherein the ether connecting group is replaced by an amino connecting group. The amino group can then be alkylated by standard procedures.

[0062] Compounds of formulae (J) and (K) wherein R⁴ is an amino group may be further treated with an alkylsulfonyl halide, e.g., methylsulfonylchloride, under basic conditions at ambient temperature to produce compounds of formulae (J) and (K) wherein R⁴ is -N(H)S(O)₂R¹².

4. Compounds of formula (M)

[0063] Compounds of formula (M), as shown below, are also intermediates in the preparation of the compounds of the invention. As illustrated below in Reaction Scheme 4, compounds of formula (M) are prepared from compounds of formula (K) and formula (L) where A is -N = or -C(R¹¹) = (where R¹¹ is hydrogen, alkyl or halo); X is fluoro of chloro; R¹ and R³ are independently hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, or -N(R⁸)C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹; R² is hydrogen, alkyl, haloalkoxy, -OR¹², -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3), -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3), -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3), -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3), -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3), morpholin-4-yl, 3-tetrahydrofuranoxy; or R² is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR¹², -C(O)N(R⁸)R⁹, halo, alkyl, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl)); or R² is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is 1-piperazinoyl (optionally substituted by one or more substituents selected from the. group consisting of alkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, alkoxycarbonyl, alkoxycarbonylalkyl, and tetrazolylalkyl); or R² is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, alkoxycarbonylalkyl and aralklyl); or R² is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, alkoxycarbonyl and alkoxycarbonylalkyl); R⁴ and R⁷ are independently hydrogen, halo, alkyl, nitro, -OR¹², -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, or -N(H)C(O)R⁸; R⁶ is halo, alkyl, haloalkyl, haloalkoxy, nitro, amino, ureido, guanidino, -OR¹², -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH₂)_mC(O)N(R⁸)R⁹ (where m is 0 to 3), -CH(OH)C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), -(CH₂)_mC(O)OR⁸ (where m is 0 to 3), -N(H)C(O)R⁸, (1,2)-tetrahydropyrimidinyl (optionally substituted by alkyl), (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl); each R⁸ and R⁹ is independently hydrogen, alkyl, aryl, or aralkyl; and R¹² is alkyl, aryl or aralkyl:

[0064] Compounds of formula (K) are prepared according to the methods described herein (see Reaction Scheme 3 above). Compounds of formula (L) are commercially available, for example, from Aldrich Chemical Co., or from Maybridge Co., or may be prepared according to methods known to those of ordinary skill in the art.

[0065] In general, the compounds of formula (M) are prepared in a manner similar to that described above for compounds of formula (J) and (K).

[0066] Compounds of formula (M) where R⁴ or R⁷ is hydroxy may be reacted with a haloalkane, such as iodomethane, under standard conditions to produce the corresponding compounds of formula (M) where R⁴ or R⁷ is alkoxy.

[0067] Compounds of formula (M) where R⁶ or R⁷ contains -C(O)OR⁸ where R⁸ is alkyl or aryl may be hydrolyzed under basic conditions (for example, in the presence of sodium hydroxide) to produce compounds of formula (M) where R⁶ or R⁷ contains -C(O)OR⁸ where R⁸ is hydrogen.

[0068] Compounds of formula (M) where the ether connecting group has been replaced by an unsubstituted amino connecting group may be treated with an alkylating agent, such as iodomethane, in the presence of a base, to produce compounds of formula (M) wherein the amino connecting group is substituted by alkyl, aryl, or aralkyl. In addition, compounds of formula (K) can be treated with a compound of formula (L) wherein the hydroxy group is replaced by a hydroxymethyl (-CH₂OH) group to produce the corresponding compounds of formula (M).

[0069] Compounds of formula (M) where each R⁶ and R⁷ independently contains -C(O)OR⁸ where R⁸ is hydrogen may be amidated or esterified under standard conditions to produce compounds of formula (M) where R⁶ or R⁷ contains -C(O)OR⁸ where R⁸ is alkyl, aryl or aralkyl, or compounds of formula (M) where R⁶ or R⁷ contains -C(O)N(R⁸)R⁹ where R⁸ and R⁹ are independently hydrogen, alkyl, aryl or aralkyl.

[0070] Compounds of formula (M) where R³ is nitro may be reduced under standard conditions to produce compounds of formula (M) where R³ is amino; which can then be reacted with the appropriate acid halide or aryl- or alkylsulfonyl halide to produce compounds of formula (M) where R³ is -N(R⁸)C(O)R⁸ or -N(R⁸)S(O)₂R¹² where R⁸ and R¹² are as defined above. In addition. compounds of formula (M) where R³ is amino can be reacted with an isocyanate or chloroformate to produce compounds of formula (M) where R³ is -N(R⁸)C(O)N(R⁸)R⁹ or -NCR⁸)C(O)OR⁸.

B. Preparation of the Compounds of the Invention

[0071] In the following Reaction Scheme 6, compounds of formula (Ia) are compounds of formula (1) as described above in the Summary of the Invention wherein Z¹ and Z² are -O-. As illustrated below in Reaction Scheme 6, wherein A is -N= R¹ and R³ is hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, -N(R⁸)R⁹, -C(O)OR¹³, -C(O)N(R⁸)R⁹, -C(O)NR⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹², or -N(R⁸)C(O)N(R⁸)CH₂-C(O)N(R⁸)R⁹; R² is hydrogen, alkyl, haloalkoxy, -OR⁸, -C(O)OR¹³, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR¹³ (where m is 0 to 3), N(R⁸)(CH₂)_nC(O)OR¹³ (where n is 1 to 3), -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR¹³ (where each n is 1 to 3), -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3), -O(CH₂)_pC(O)OR¹³ (where p is 1 to 6), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR¹³ (where each n is independently 1 to 3), morpholin-4-yl, 3-tetrahydrofuranoxy; or R² is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl. (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl)); or R² is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl); or R² is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyi, and tetrazolylalkyl); or R² is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl and aralklyl); or R² is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl); R⁴ and R⁷ are independently hydrogen, halo, alkyl, nitro, -OR⁸, -C(O)OR¹³, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, or -N(H)C(O)R⁸; R⁶ is halo, alkyl, haloalkyl, haloalkoxy, nitro, amino, ureido, guanidino, -OR⁸, -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH₂)_mC(O)N(R⁸)R⁹ (where m is 0 to 3), -CH(OH)C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), -(CH₂)_mC(O)OR¹³ (where m is 0 to 3), -N(H)C(O)R⁸, (1,2)-tetrahydropyrimidinyl (optionally substituted by alkyl), (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl); each R⁸ and R⁹ is independently hydrogen, alkyl, aryl, or aralkyl; R¹⁰ is hydrogen, alkyl, aryl, aralkyl, 1-pyrrolidinyl, 4-morpholinyl, 4-piperazinyl, 4-(N-methyl)piperazinyl, or 1-piperidinyl; R¹² is alkyl, aryl or aralkyl; and R¹³ is hydrogen, alkyl or aralkyl; compounds of formula (Ia) are prepared from compounds of formula (Q) as follows:

[0072] Compounds of formula (Q) are prepared as described herein above for compounds of formulae (J), (M), and (P).

[0073] In general, compounds of formula (Ia) are prepared from compounds of formula (Q) by dissolving the compound of formula (Q) in an anhydrous alkanol, preferably ethanol and then treating the solution with an anhydrous mineral acid, preferably HCI, while maintaining the reaction temperatures between about -78°C and ambient temperature for between 2 hours and 24 hours, allowing the temperature to rise to ambient temperature while monitoring for reaction completion, for example, through thin layer chromatography. The solvent is then removed and the resulting residue dissolved in fresh anhydrous alkanol, preferably ethanol. The resulting solution was then treated with anhydrous ammonia at ambient pressure or in a sealed flask, at temperatures from between ambient temperature and 100°C for about 1 to about 5 hours. The compounds of formula (Ia) are then isolated from the reaction mixture by standard techniques.

[0074] Compounds of formula (Ia) wherein R⁶ is -C(NH)NH₂ or -C(NH)NHOH are produced from the corresponding cyano compounds.

[0075] Alternatively, instead of treating the resulting residue above with anhydrous ammonia, the resulting residue may be treated with a compound of the formula NH₂OR⁸ to afford the corresponding compound of formula (Ia) wherein R⁵ is -C(NH)N(H)OR⁸.

[0076] In addition, compounds of formula (Ia) which contain a -C(O)OR¹³ group may be treated under standard transesterification conditions with an phenol or a naphthol (either optionally substituted by halo, alkyl, alkoxy, amino, nitro or carboxy) to produce compounds of the invention which contain a -C(O)OR⁸ group where R⁸ is aryl.

[0077] Compounds of formula (Ia) wherein R⁶ is -C(NH)NH₂ or -C(NH)N(H)OR¹³ are produced from the corresponding cyano compounds in a similar manner as that described above for the compounds of formula (Ia).

[0078] In addition, compounds of formula (Ia) where R¹, R², R³, R⁴, and R⁷ contains a -N(R⁸)R⁹ group where R⁸ and R⁹ are hydrogen, can be treated with the appropriate alkylating agents to afford the corresponding compounds of formula (Ia) where R¹, R², R³, R⁴, and R⁷ contains -N(R⁸)R⁹-N(R⁸)S(O)₂R¹², -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)CH₂-C(O)N(R⁸)R⁹, or -NCR⁸)C(O)R⁸ where each R⁸ and R⁹ is independently hydrogen, alkyl, aryl or aralkyl, and R¹² is alkyl, aryl or aralkyl.

[0079] Compounds of formula (Ia) may be further treated with the appropriate acid halide, preferably acid chloride, or with the appropriate acid anhydride or an equivalent, to yield compounds of the invention wherein R⁵ is -C(NH)N(H)C(O)R⁸ where R⁸ is hydrogen, alkyl, aryl or aralkyl.

[0080] Alternatively, compounds of formula (Ia) may further be treated with carbamoyl chlorides or their equivalents to yield compounds of the invention where R⁵ is -C(NH)N(H)C(O)OR¹² where R¹² is alkyl, aryl or aralkyl.

[0081] Alternatively, compounds of formula (Ia) may be further treated with compounds of the formula R¹²-S(O)₂-imidazole where R¹⁶ is described in the Summary of the Invention in a polar solvent, such as methylene choride, at ambient temperature to afford compounds of the invention where R⁵ is -C(NH)N(H)S(O)₂R¹².

[0082] Alternatively, compounds of formula (Ia) may be further treated with an appropriatly N-R⁹-substituted phenylcarbamate in a polar solvent, preferably methylene chloride, at ambient temperature, for about 6 to 24 hours, preferably for about 12 hours, to afford compounds of the invention where R⁵ is -C(NH)N(H)C(O)N(R⁸)R⁹.

[0083] Compounds of formula (Ia) wherein R¹, R² or R³ contains -C(O)N(R⁸)R⁹ or -C(O)OR¹³ where each R⁸ and R⁹ are independently alkyl, haloalkyl, aryl or aralkyl, and R¹³ is alkyl or aralkyl may be hydrolyzed under acidic conditions to prepare compounds of formula (Ia) where R¹, R² or R³ contains -C(O)OR⁸ where R⁸ is hydrogen.

[0084] Under the same conditions as previously described, compounds of formula (Ia) where R¹, R² or R³ contains -C(O)OR¹³ where R¹³ is hydrogen, alkyl, or aralkyl, may be amidated to form compounds of formula (Ia) where R¹, R² or R³ contains -C(O)N(R⁸)R⁹ where R⁸ and R⁹ are independently hydrogen, alkyl, aryl or aralkyl.

[0085] Compounds of formula (Ia) where R⁴ is -OR⁸ where R⁸ is alkyl, aryl or aralkyl, may be converted to compounds of formula (Ia) where R⁴ is -OR⁸ where R⁸ is hydrogen by treatment with boron tribromide in an aprotic solvent, for example, methylene chloride, at temperatures at first between -80°C and 0°C, then at ambient temperature, for about 4 hours to about 16 hours.

[0086] Alternatively, compounds of formula (Ia) where R⁴ is -OR⁸ where R⁸ is arylmethyl, preferably, benzyl, may be treated with hydrogen and the appropriate catalyst, for example, palladium on carbon, to give compounds of formula (Ia) where R⁴ is -OR⁸ where R⁸ is hydrogen.

[0087] Compounds of formula (Ia) where R² is 3-pyrrolidinyloxy substituted by arylmethyl on the nitrogen may be treated under standard hydrogenolysis conditions to remove the arylmethyl group to produce compounds of formula (Ia) where R² is unsubstituted 3-pyrrolidinyloxy, which can then be reacted with the appropriate imidate to produce the compounds of formula (Ia) where R² is 3-pyrrolidinyloxy substituted by 1-iminoethyl, or with the appropriate haloalkyl esters to produce the compounds of formula (Ia) where R² is 3-pyrrolidinyloxy substituted by alkoxycarbonylalkyl.

[0088] In summary, compounds of the invention, are prepared by:

1) reacting a compound of formula (A) as described above with a compound of formula (B) as described above under the conditions as described above to produce a compound of formula (C) as described above, which is an intermediate in the preparation of the compounds of the invention; or

2) reacting a compound of formula (D) as described above with a compound of formula (E) as described above under conditions as described above to produce a compound of formula (F) as described above, which is an intermediate in the preparation of the compounds of the invention; or

3) reacting a compound of formula (G) as described above, which can be a compound of formula (C) as described above or a compound of formula (F) as described above, with a compound of formula (H) as described above under conditions as described above to produce a compound of formula (J) or a compound of formula (K) as described above, which are intermediates in the preparation of the compounds of the invention; then

4) reacting a compound of formula (K) as described above with a compound of formula (L) as described above under conditions as described above to produce a compound of formula (M) as described above, which is an intermediate in the preparation of the compounds of the invention;

5) reacting a compound of formula (Q) as described above, which can be a compound of formula (J), a compound of formula (M) as described above, with the appropriate reagent under the conditions as described above to form compounds of formula (Ia) as described above.

[0089] Similar reactions may be performed on similar starting materials and intermediates to produce the corresponding compounds of the inventions not depicted in the Reaction Schemes above.

[0090] In addition, all compounds of the invention that exist in free base form or free acid form may be converted to their pharmaceutically acceptable salts by treatment with the appropriate inorganic or organic acid, or by the appropriate inorganic or organic base. Salts of the compounds of the invention can also be converted to the free base form or to the free acid form or to another salt.

PREPARATION 1

4-Methoxy-2,3,5,6-tetrafluoropyridine

[0091] 

A. To pentafluoropyridine (1.0 g, 5.9 mmol) in petroleum ether (60 mL) at 0°C was added sodium methoxide (0.32 mg, 5.9 mmol). After stirring for 12 hours at ambient temperature, the reaction was washed with water, dried (MgSO₄), and the solvent was removed in vacuo to give 4-methoxy-2,3,5,6-tetrafluoropyridine; NMR (CDCl₃) 4.3 ppm. .

B. In a similar manner, the following compounds were made: 2,3,5,6-tetrafluoro-4-(2,2,2-trifluoroethoxy)pyridine; and 2,3.5 ,6-tetrafluoro-4-(1,3-difluoroprop-2-oxy)pyridine.

PREPARATION 2

[0092] 4-Dimethylamino-2,3,5,6-tetrafluoropyridine

A. To methylene chloride (50 mL) cooled in an ice bath was added pentafluoropyridine (2.0 g, 11.8 mmol) and dimethylamine (2.97 mL of a 40% solution in water, 24 mmol). After stirring for 30 minutes the solution was washed with water, and dried over basic alumina. The solvent was removed in vacuo to give 4-dimethylamino-2,3,5,6-tetrafluoropyridine; NMR (CDCl₃) 3.13 (m,6) ppm.

B. In a similar manner, the following compounds were made:

1-(2,3,5,6-tetrafluoropyridin-4-yl)piperidine-4-carboxylic acid, ethyl ester; NMR (CDCI₃) 4.15 (q,2), 3.7 (m,2), 3.25 (m,2), 2.55 (m,1), 2.05 (m,2), 1.9 (m,2), 1.15 (t,3) ppm;

1-(2,3,5,6-tetrafluoropyridin-4-yl)piperidine-3-carboxylic acid, ethyl ester; NMR (CDCl₃) 4.15 (q,2), 3.8 (m,1), 3.55 (m,1), 3.4 (m,1), 3.25 (m,1), 2.7 (m,1), 2.15 (m,1), 1.8 (m,3), 1.15 (t,3) ppm;

4-(piperidin-1-yl)-2,3,5,6-tetrafluoropyridine; NMR (CDCl₃) 3.4 (m,4), 1.7 (m,6) ppm;

4-(4-methylpiperazin-1-yl)-2,3,5,6-tetrafluoropyridine; NMR (CDCl₃) 3.45 (m,4), 2.5 (m,4), 2.3 (s,3) ppm;

4-(2,3,5,6-tetrafluoropyridin-4-yl)piperazine-1-acetic acid, ethyl ester; NMR (CDCI3) 4.2 (q,2), 3.55 (m,4), 3.3 (s,2), 2.7 (m,4), 1.3 (t,3) ppm;

N-methyl-N-(2,3,5,6-tetrafluoropyridin-4-yl)glycine, ethyl ester; and

4-(morpholin-1-yl)-2,3,5,6-tetrafluoropyridine.

PREPARATION 3

1-[(2,6-Dichloropyridin-4-yl)carbonyl]-4-methylpiperazine, Hydrochloride

[0093] To methylene chloride (15 mL) was added 2,6-dichloropyridine-4-carbonyl chloride (1.0 g, 4.8 mmol) and 1-methylpiperazine (0.48 g, 4.8 mmol). After stirring for 1 day, the reaction was poured into ether. The resulting solid was filtered to give 1-[(2,6-dichloropyridin-4-yl)-carbonyl]-4-methylpiperazine, hydrochloride.

PREPARATION 4

3-(1-Methylimidazolin-2-yl)phenol, Hydrobromide

[0094] 

A. To ethanol (200 mL) was added 3-methoxybenzonitrile (10.9 g, 82 mmol). The solution was cooled in an ice bath and HCI (g) was bubbled into the solution. The reaction was warmed to ambient temperature and stirred for 2 days. The solvent was removed in vacuo and the residue was slurried in ethanol (20 mL). N-methylethylene--diamine (12 g, 160 mmol) was added and the reaction was refluxed for 7 hours. The solvent was removed in vacuo and the residue was chromatographed on silica gel with methylene chloride/methanol/ammonium hydroxide (20/1/0.1). The resulting oil was dissolved in 48% HBr (20 mL) and refluxed for 19 hours. The mixture was cooled to ambient temperature and the solvent was removed in vacuo to give 3-(1-methylimidazolin-2-yl)phenol, hydrobromide.

B. In a similar manner, the following compound is made:

3-(1-methyltetrahydropyrimidin-2-yl)phenol, hydrobromide.

PREPARATION 5

3,3'-[2,6-Pyridinediylbis(oxy)]bis(benzonitrile)

[0095] 

A. To sodium hydride (0.38 g, 9.5 mmol) in N,N-dimethylformamide (3 mL) was added 3-cyanophenol (1.1 g, 8.9 mmol) and 2,6-difluoropyridine (0.4 mL, 4.4 mmol). After heating in an on bath at 100°C for 15 hours the reaction was partitioned with ethyl acetate and water. The organic layer was separated, washed with water, dried (Na₂SO₄), and the solvent was removed in vacuo. The residue was chromatographed on silica gel (50 g) with methylene chloride/hexane (3/1) to give 3,3'-[2,6-pyridinediylbis(oxy)]bis(benzonitrile). Recrystallization from ethyl acetate/hexane gave pure 3,3'-[2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.79 (t,1), 7.45 (m,4), 7.32 (m.4), 6.72 (d.2) ppm.

B. In a similar manner, the following compounds were made:

4,4'-[2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.8 (t,1), 7.6 (d,4), 7.2 (d,4), 6.8 (d,2) ppm;

3,3'-[3,5-dichloro-2,6-pyridinediylbis(oxy)]bislbenzonitrile); NMR (CDCl₃) 7.9 (s,1), 7.45 (m,4), 7.2 (m,4) ppm;

4,4'-(3,5-dichloro-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.95 (s,1), 7.6 (d,4), 7.1 (d,4) ppm;

2,6-bis(3-cyanophenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.45 (m,4), 7.35 (m,6), 4.45 (q,2), 1.45 (t,3) ppm;

2,6-bis(3-cyanophenoxy)pyridine-3-carboxylic acid, ethyl ester; NMR (CDCl₃) 8.4 (d,1), 7.45 (m,4), 7.25 (m,4), 6.75 (d,1), 4.4 (q,2), 1.45 (t,3) ppm;

3,3'-(3,5-difluoro-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.55 (t,1), 7.45 (m,4), 7.29 (m,4) ppm;

3,3'-(2,6-pyrazinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 8.2 (s,2), 7.5 (m,4), 7.3 (m,4) ppm;

3,3'-[2,6-pyrimidinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 8.4 (d,1), 7.5 (m,4), 7.4 (m,4), 6.8 (d,1) ppm;

3,3'-[3,5-difluoro-4-methyl-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.44 (m,4), 7.27 (m,4), 2.4 (s,3) ppm;

3,3'-[4-nitro-1,3-phenylenebis(oxy)]bis(benzonitrile); NMR (CDCl₃) 8.13 (d,1) 7.5 (m,4), 7.3 (m,4), 6.84 (dd,1), 6.69 (d,1) ppm; and

3.3'-[3-trifluoromethyl-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 8.05 (t,1), 7.5 (m,4), 7.3 (m,4), 6.8 (d,1) ppm.

PREPARATION 6

[0096] 3-[(3,5,6-Trifluoro-4-methylpyridin-2-yl)oxy]benzonitrile

A. To 2,3,5,6-tetrafluoro-4-methylpyridine (0.71 g, 4.3 mmol) dissolved in acetonitrile (5 mL) was added 3-cyanophenol (0.5 g, 4.2 mmol) and cesium carbonate (1.449,4.4 mmol). The reaction was heated in an oil bath at 45 °C for 16 hours and partitioned with ether and water. The organic layer was separated, washed with brine, dried (Na₂SO₄), and the solvent removed in vacuo. Chromatography on silica gel with methylene chloride/hexane (7/3) gave 3-[(3,5,6-trifluoro-4-methylpyridin-2-yl)-oxy]benzonitrile; NMR (CDCl₃) 7.55 (m,2), 7.45 (m,2), 2.24 (s,3) ppm.

B. In a similar manner, the following compounds were made:

4-[(2,3,5,6-tetrafluoropyridin-4-yl)oxy]-3-methoxybenzoic acid, ethyl ester;

3-(4-dimethylamino-3,5,6-trifluoropyridin-2-yl)-4-methoxybenzonitrile; NMR (CDCl₃) 7.55 (d,1), 7.4 (s,1), 7.05 (d,3), 3.85 (s,3), 3.15 (s,6) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-3,5,6-trifluoropyridin-4-yl)piperidine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.5 (d,1), 7.4 (s,1), 7.05 (d,1), 4.15 (q,2), 3.8 (s,3), 3.7 (m,2), 3.25 (m,2), 2.55 (m,1), 2.1 (m,2), 1.9 (m,2), 1.15 (t,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-3,5,6-trifluoropyridin-4-yl)piperidine-3-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.5 (d,1), 7.4 (s,1), 7.05 (d,1), 4.15 (q,2), 3.8 (s,3), 3.8 (m,1), 3.55 (m, 1), 3.4 (m,1), 3.25 (m,1), 2.7 (m,1), 2.15 (m,1), 1.8 (m,3), 1.15 (t,3) ppm;

2-chloro-6-(5-cyano-2-methoxyphenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.6 (m,2), 7.4 (m,2), 7.0 (d,2), 4.4 (q,2), 3.8 (s,3), 1.4 (t,3) ppm;

2-chloro-6-(3-dimethylaminophenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.6 (s,1), 7.2 (m,2), 6.6 (d,1), 6.5 (m,2), 4.4 (q,2), 3.0 (s,6), 1.4 (t,3) ppm;

4-benzyloxy-3-(4-(piperidin-1-yl)-3,5,6-trifluoropyridin-2-yl)benzonitrile; NMR (CDCl₃) 7.5 (m,2), 7.35 (m,3), 7.2 (m,2), 7.05 (d,1), 5.1 (s,2), 3.4 (m,4), 1.75 (m,6) ppm;

4-benzyloxy-3-(4-(4-methylpiperazin-1-yl)-3,5,6-trifluoropyridin-2-yl)benzonitrile; NMR (CDCl₃) 7.5 (m,2), 7.35 (m,3), 7.2 (m,2), 7.05 (d,1), 5.1 (s,2), 3.4 (m,4), 2.5 (m,4), 2.35 (s,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-6-chloropyridin-4-yl)carbonyl)-4-methylpiperazine; NMR (CDCl₃) 7.44 (dd,1), 7.3 (d,1), 6.95 (d,1), 6.9 (s,1), 6.74 (s,1), 3.7 (s,3), 3.7 (m,2), 3.3 (m,21, 2.4 (m,2), 2.3 (m,2), 2.2 (s,3) ppm;

4-[(2-(5-cyano-2-benzyloxyphenoxy)-3,5,6-trifluoropyridin-4-yl)piperazine-1-acetic acid, ethyl ester; NMR (CDCI₃) 7.5 (m,2), 7.35 (m,3), 7.2 (m,2), 7.05 (d,1), 5.1 (s,2), 4.2 (q,2), 3.5 (m,4), 3.3 (s,2), 2.75 (m,4), 1.3 (t,3) ppm;

3-[(3,5,6-trifluoro-4-methylpyridin-2-yl)oxy]-4-methoxybenzonitrile; NMR (CDCI₃) 7.6 (d,1), 7.4 (s,1), 7.0 (d,1), 3.8 (s,3), 2.4 (s,3) ppm;

3-[(3,5,6-trifluoro-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCI₃) 7.4 (m,1), 7.2 (d,1), 7.3 (m,1), 7.1-7.2 (m,2), 4.7 (q,2), 3.1 (s,3), 3.0 (s,3) ppm;

3-[(4-(1,3-difluoroprop-2-oxy)-3,5,6-trifluoropyridin-2-yl)oxy]-N, N-dimethylbenzamide;

N-(2-(5-cyano-2-methoxyphenoxy)-3,5,6-trifiuoropyridin-4-yl)-N-methylglycine, ethyl ester;

N-(2-(3-cyanophenoxy)-3,5,6-trifluoropyridin-4-yl)-N-methylglycine, ethyl ester;

3-(4-(morpholin-1-yl)-3,5,6-trifluoropyridin-2-yl)oxy)-4-[benzyloxy)benzonitrile;

2-chloro-6-(3-dimethylaminocarbonylphenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.59 (s,1), 7.46 (t,1), 7.38 (s,1), 7.32 (d,1), 7.21 (s,1), 7.2 (d,1), 4.42 (q,2), 3.05 (s,3), 2.88 (s,3), 1.20 (t,3) ppm;

3-[(6-fluoropyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.75 (q,1), 7.43 (m,1), 7.27 (m,1), 7.2 (m,2), 6.75 (m,1), 6.62 (d,1), 3.1 (s,3), 3.0 (s,3) ppm;

4-[(2-(5-cyano-2-benzyloxyphenoxy)-3,5,6-trifluoropyridin-4-yl)oxy]-3-methoxybenzoic acid, ethyl ester; and

4-[(2-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-4-yl)oxy]-3-methoxybenzoic acid, ethyl ester.

PREPARATION 7

3-[(3,5-Difluoro-6-(5-dimethylamino-2-methylphenoxy)-4-methyl-pyridin-2-yl)oxy]benzonitrile

[0097] 

A. In a manner similar to preparation 6, reaction of 3-(3,5,6-trifluoro-4-methylpyridin-2-yl)benzonitrile (1.1 g, 4.4 mmol), 5-dimethylamino-2-methylphenol (0.66 g, 4.4 mmol), and cesium carbonate (1.7 g, 5.2 mmol) in acetonitrile (10 mL) gave 3-[(3,5-difluoro-6-(5-dimethylamino-2-methylphenoxy)-4-methylpyridin-2-yl)oxy]-benzonitrile; NMR (CDCl₃) 7.3 (m,4), 7.0 (d,1), 6.5 (d,1), 6.3 (s,1), 2.8 (s,6), 2.4 (s,3), 2.0 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3-[(3,5-difluoro-6-(3-dimethylamino-2-methylphenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.1-7.5 (m,5), 6.9 (d,1), 6.65 (d,1), 6.3 (s,1), 2.6 (s,6), 2.4 (s,3), 2.0 (s,3) ppm;

3,3'-[3,5-difluoro-4-methoxy-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR CDCl₃) 7.45 (m,4), 7.3 (m,4), 4.3 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-4-methoxybenzenecarboxylic acid; NMR (CDCl₃) 7.9 (d,1), 7.7 (s,1), 7.2 (m,4), 6.95 (d,1), 3.85 (s,3), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-4,5-dimethoxybenzenecarboxylic acid, ethyl ester; NMR (CDCl₃) 7.4 (s,1), 7.2-7.4 (m,5), 4.35 (q,2), 3.9 (s,3), 3.8 (s,3), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-4-methylbenzoic acid; NMR (CDCl₃) 7.75 (d,1), 7.55 (s,1), 7.1-7.3 (m,5), 2.4 (s,3), 2.2 (s,3) ppm;

5-[6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-1,3-dicarboxylic acid, diethyl ester; NMR (CDCl₃) 8.45 (s,1), 7.85 (s,2), 7.25 (m,4), 4.4 (q,4), 2.4 (s,3), 1.4 (t,6) ppm;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-3-methoxybenzoic acid; NMR (CDCl₃) 7.65 (dd,1), 7.62 (d,1), 7.33 (dt,1), 7.27 (dt,1), 7.18 (m,2), 7.05 (d,1), 3.8 (s,3), 2.4 (s,3) ppm;

3,3'-[3-nitro-2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 8.6 (d,1), 7.5 (m,4), 7.2 (m,4), 6.8 (d,1) ppm;

3-[(3,5-difluoro-6-(4-dimethylaminomethylphenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.3 (m,5), 7.15 (m,1), 6.9 (m,2), 3.35 (s,2), 2.4 (s,3), 2.15 (s,6) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(morpholin-4-yl)phenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.1-7.4 (m,5), 6.7 (d,1), 6.5 (s,1), 3.8 (m,4), 3.1 (m,4), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-(2-(1H-imidazol-1-yl)-1-oxoethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.8 (d,1), 7.7 (s,1), 7.5 (m,2), 7.3 (m,5), 7.1 (s,1), 7.0 (s,1), 5.45 (s,2), 2.4 (s,3) ppm;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoic acid; NMR (CDCl₃) 8.05 (d,2) 7.2-7.5 (m,4), 7.1 (d,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-((phenyl)oxomethyl)phenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.75 (d,2), 7.4-7.6 (m,6), 7.3 (m,5); 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-hydroxyphenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.35 (m,4), 7.2 (t,1), 6.65 (dd,1), 6.6 (m,2), 5.65 (s,1), 2.4 (s,3) ppm;

5-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-2-methoxybenzonitrile; NMR (CDCl₃) 7.4 (d,1), 7.3 (s,1), 7.03 (t,1), 6.8 (d,1), 6.43 (d,1), 6.25 (s,1), 6.18 (d,1), 3.68 (s,3), 2.85 (s,6), 2.45 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzeneacetic acid, ethyl ester; NMR (CDCl₃) 7.3 (m,5), 7.05 (d,1), 6.9 (m,2), 3.65 (s,3). 3.6 (s,2), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzenepropionic acid; NMR (CDCl₃) 7.3 (m,5), 7.05 (d,1), 6.85 (m,2), 2.9 (t,2), 2.6 (t,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-2,6-dimethoxybenzonitrile; NMR (CDCl₃) 7.3 (d,1), 7.0 (t,1), 6.55 (d,1), 6.4 (d,1), 6.2 (m,2), 3.9 (s,3), 3.7 (s,3), 2.9 (s,6), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-(2-hydroxyethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.2-7.4 (m,5), 7.0 (d,1), 6.85 (m,2), 3.75 (t,2), 2.8 (t,2), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzenepropionamide; NMR (CDCI₃) 7.45 (d,1), 7.1-7.4 (t,4), 7.0 (d,1), 6.85 (m,1), 6.8 (d,1), 3.9 (s,3), 3.85 (s,3), 3.85 (m,2), 2.5 (t,2), 2.35 (s,3) ppm;

3-[(3,5-difluoro-6-(3-(hydroxymethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.3-7.5 (m,5), 7.2 (d,1), 7.1 (s,1), 6.95 (d,1), 4.7 (s,2), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCI₃) 7.2-7.4 (m,5), 7.0 (m,1), 6.9 (m,2), 3.65 (s,2), 2.95 (s,6), 2.35 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCI₃) 7.35 (m.2), 7.25 (m,2), 7.2 (t,1), 7.0 (d,1), 6.85 (m,2), 2.9 (t,2), 2.45 (t,2), 2.4 (s,3) ppm;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-α-hydroxybenzeneacetic acid; NMR (CDCl₃) 7.25 (m,6), 7.15 (s,1), 6.95 (m,1), 5.2 (s,1), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(1-oxoethyl)phenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCI₃) 7.75 (dt,1), 7.59 (m,1), 7.44 (t,1), 7.2-7.4 (m,5), 2.57 (s,3), 2.40 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(2-methyl-1-oxopropyl)phenoxy) pyridin-2-yl)oxy]-benzonitrile; NMR (CDCl₃) 7.75 (d,1), 7.6 (m,1), 7.45 (t,1), 7.2-7.4 (m,5), 3.45 (m,1), 2..4 (s,3), 1.25 (m,6) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(1-methylethoxy)phenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.2-7.5 (m,5), 6.7 (d,1), 6.55 (m,2), 4.45 (m,1), 2.4 (s,3), 1.3 (m,6) ppm;

α-acetoxy-4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzeneacetamide; NMR (CDCl₃) 7.3 (m,6), 7.15 (m,1), 7.0 (m,1), 6.1 (s,1), 2.9 (s,3), 2.85 (s,3), 2.40 (s,3), 2.1 (s,3) ppm;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-α-ethoxybenzeneacetic acid, methyl ester; NMR (CDCl₃) 7.0-7.5 (m,8), 4.75 (s,1), 3.75 (s,3), 3.35 (s,3), 2.4 (s,3) ppm;

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-dimethylaminopyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.4 (m,2), 7.1 (d,1), 6.95 (m,3), 3.8 (s,3), 3.1 (s,6), 3.05 (s,3), 2.9 (s,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)pyridin-4-yl]piperidine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.4 (d,1), 7.2 (m,2), 7.1 (d,1), 6.9 (m,3), 4.15 (q,2), 3.75 (s,3), 3.7 (m,2), 3.25 (m,2), 3.1 (s,3), 2.95 (s,3), 2.55 (m,1), 2.0 (m,4), 1.15 (t,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)pyridin-4-yl]piperidine-3-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.4 (d,1), 7.3 (m,2), 7.1 (d,1), 6.9 (m,3), 4.15 (q,2), 3.8 (m,1), 3.75 (s,3), 3.6 (m,1), 3.4 (m,1), 3.25 (m,1), 3.1 (s,3), 2.9 (s,3), 2.7 (m,1), 2.15 (m,1), 1.8 (m,3), 1.15 (t,3) ppm;

3-[(6-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoro-4-(piperidin-1-yl)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.4 (m,5), 7.2 (m,3), 7.1 (m,1), 6.95 (m,3), 5.1 (s,2), 3.4 (m,4), 3.1 (s,3), 2.9 (s,3), 1.75 (m,6) ppm;

3-[(6-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoro-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.2 (m,9), 6.95 (m,3), 5.1 (s,2), 3.5 (m,4), 3.1 (s,3), 2.9 (s,3), 2.6 (m,4), 2.4 (s,3) ppm;

4-[(2-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoro-6-(3-dimethylaminocarbonylphenoxylpyridin-4-yl]piperazine-1-acetic acid, ethyl ester; NMR (CDCl₃) 7.3 (m,5), 7.15 (m,4), 6.95 (m,3), 5.1 (s,2), 4.2 (q,2), 3.5 (m,4), 3.3 (s,2), 3.1 (s,3), 2.8 (s,3), 2.75 (m,4), 1.3 (t,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxy)-6-(3-dimethylaminocarbonylphenoxy)pyridin-4-yl)carbonyl]-4-methylpiperazine; NMR (CDCl₃) 7.4 (dd,1), 7.27 (m,2), 7.16 (m,1), 7.0 (m,2). 6.9 (d,1), 6.63 (s,1), 6.55 (s,1), 3.8 (m,2), 3.8 (s,3), 3.5 (m,2), 3.1 (s,3), 2.9 (s,3), 2.5 (m,2), 2.4 (m,2), 2.4 (s,3) ppm;

1-[(2-(5-cyano-2-methoxyphenoxyl-6-chloropyridin-4-yl)carbonyl]-4-methylpiperazine; NMR (CDCl₃) 7.44 (dd,1), 7.3 (d,1), 6.95 (d,1), 6.9 (s,1), 6.74 (s,1), 3.7 (s,3), 3.7 (m,2), 3.3 (m,2), 2.4 (m,2), 2.3 (m,2), 2.2 (s,3) ppm;

2-(5-cyano-2-methoxyphenoxy)-6-(3-(imidazol-1-yl)phenoxylpyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.8 (s,1), 7.3 (m,3), 7.2 (m,5), 7.0 (m,2), 6.7 (d,1), 4.4 (q,2), 3.7 (s.3), 1.4 (t,3) ppm;

2-(5-cyano-2-methoxyphenoxy)-6-(3-dimethylaminophenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.4 (d,1), 7.3 (s,1), 7.2 (s,1), 7.1 (t,1), 7.0 (s,1), 6.8 (d,1), 6.5 (d,1), 6.3 (m,2), 4.4 (q,2), 3.7 (s,3), 2.8 (s,6), 1.4 (t,3) ppm;

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 8.00 (bs,1), 7.40 (dt,1), 7.25 (t,1), 7.21 (dt,1), 7.08 (bd,1), 6.91 (bs,1), 6.87 (td,1), 3.74 (s,3), 2.92 (s,3), 2.85 (s,3), 2.39 (s,3) ppm;

3-[(6-(2-amino-5-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.5 (t,1), 7.2-7.0 (m,5), 6.6 (d,1), 4.6 (s,2), 3.1 (s,3), 2.9 (s,3), 2.0 (s,3) ppm;

3-[(6-(2-amino-5-cyanophenoxy)-3,5-difluoro-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.3 (dd,1), 7.2 (d,1), 7.1 (m,2), 7.0-7.1 (m,2), 6.6 (d,1), 4.8 (q,2), 4.6 (s,2), 3.1 (s,3), 2.9 (s,3) ppm;

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.4 (dd,1), 7.3 (d,1), 7.2 (t,1), 7.1 (d,1), 6.9-7.0 (m,2), 6.9 (d,1), 4.7 (q,2), 3.7 (s,3), 3.1 (s,3), 2.9 (s,3) ppm; and

3-[(6-(5-cyano-2-methoxyphenox)-4-(1,3-difluoroprop-2-oxy)-3,5-difluoropyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.4 (dd,1), 7.3 (d,1), 7.2 (t,1), 7.1 (d,1), 6.9-7.0 (m,2), 6.9 (d,1), 5.0 (m,1), 4.9 (d,2), 4.7 (d,2), 3.7 (s,3), 3.1 (s,3), 2.9 (s,3) ppm.

PREPARATION 8

4-(6-Fluoropyridin-2-yl)oxy-3-methoxybenzonitrile

[0098] 

A. To 4-hydroxy-3-methoxybenzonitrile (2.6 g, 17 mmol) in DMSO (15 mL) was added sodium hydride (0.44 g, 18 mmol) and 2,6-difluoropyridine (1.0 g, 8.7 mmol). After heating at 100°C for 18 hours the reaction was partitioned with ethyl acetate and water. The organic layer was separated, washed with water, dried (Na₂SO₄), and the solvent was removed in vacuo to give 4-(6-fluoropyridin-2-yl)oxy-3-methoxybenzonitrile (1.3 g); NMR (CDCl₃) 7.8 (q,1), 7.35 (m,1), 7.25 (m,2), 6.85 (d,1), 6.65 (m,1), 3.85 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3-[(4-methyl-3,5,6-trifluoropyridin-2-yl)amino]benzonitrile; NMR (CDCl₃) 8.05 (s,1), 8.95 (d,1), 7.6 (d,1), 7.45 (t,1), 7.25 (s,1), 2.3 (s,3) ppm;

2-chloro-6-(3-cyanophenoxy)pyridine-4-carboxylic acid, ethyl ester, NMR (CDCl₃) 7.80-7.38 (m,6), 4.41 (q,2), 1.92 (t,3) ppm;

2-chloro-6-(5-cyano-2-methoxyphenoxy)-N,N-dimethylpyridine-4-carboxamide; NMR (CDCl₃) 7.2 (m,5), 3.84 (s,3), 3.13 (s,3), 2.95 (s,3) ppm; and

2-chloro-6-(5-cyanophenoxy)-N,N-dimethylpyridine-4-carboxamide; NMR (CDCI3) 7.45 (m,3), 7.08 (s,1), 6.87 (s,1), 6.67 (s,1), 3.14 (s,3), 3.00 (s,3) ppm.

PREPARATION 9

[0099] 2-Methoxy-3',4-[2,6-pyridinediylbis(oxy)]benzonitrile

A. To 4-(6-fluoropyridin-2-yl)oxy-3-methoxybenzonitrile (0.65 g, 2.7 mmol) in DMSO (1 5 mL) was added 3-cyanophenol (0.32 g, 0.91 mmol) and sodium hydride (0.070 g, 2.9 mmol). After heating at 140 °C for 2 days, the reaction was poured into water and the precipitate was filtered off. The solid was chromatographed to give 2-methoxy-3',4-[2,6-pyridinediylbis(oxy)]benzonitrile; NMR (CDCI₃) 7.75 (t,1), 7.2-7.5 (m,6), 7.1 (d,1), 6.7 (d,1), 6.65 (d,1), 3.8 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3,3'-bis(methoxy)-4,4'-[2,6-pyridinediylbisloxy)]bis(benzonitrile); NMR (CDCI₃) 7.75 (t,1), 7.2 (d,2), 7.1 (m,4), 6.65 (d,2), 3.75 (s,6) ppm;

3-[(3,5-difluoro-6-(3-ethylamino-4-methylphenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCI₃) 7.3 (m,4), 6.95 (d,1), 6.25 (m,2), 3.45 (br s,1), 3.1 (q,2), 2.4 (s,3), 2.1 (s,3), 1.3 (t,3) ppm;

3,4'-[2,6-pyridinediylbis(oxy)]bis(benzonitrile); NMR (CDCl₃) 7.8 (t,1), 7.6 (d,2), 7.2-7.5 (m,4), 7.14 (d,2), 6.7 (d,2) ppm;

3-[(6-[(3-cyanophenyl)amino]-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCI₃) 7.65 (m,2), 7.5 (m,2), 7.2-7.4 (m,4), 2.4 (s,3) ppm;

3-[6-(3-cyanophenyl)amino-3,5-difluoro-4-methylpyridin-2-yl(methylamino)]-benzonitrile; NMR (CDC:3) 7.1-7.5 (m,9), 3.4 (s,3), 2.3 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(pyridin-3-yloxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 8.4 (m,2), 7.35 (m,4), 7.25 (m,4), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-phenoxypyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.25-7.5 (m,6), 7.2 (t,1), 7.0 (d,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(4-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.25-7.5 (m,4), 6.95 (d,2), 6.65 (d,2), 2.95 (s,6). 2.4 (s,3) ppm;

3-[(6-(3,5-difluoro-6-(3-(1H-imidazol-1-yl)phenoxy)-4-methylpyridin-2-yl)oxy]-benzonitrile; NMR (CDCl₃) 7.75 (s,1), 7.4 (t,1), 7.1-7.3 (m,7), 7.03 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-nitrophenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 8.03 (d,1), 7.85 (s,1), 7.5 (t,1), 7.4 (m,3), 7.3 (m,2), 2.4 (s,3) ppm;

3[(6-(3-aminophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCI₃) 7.35 (m,4), 7.05 (1,1), 6.45 (d,1), 6.35 (m,2), 2.4 (s,3) ppm;

N-[3-(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy)phenoxy]acetamide; NMR (CDCI₃) 7.55 (m,2). 7.2-7.4 (m,5), 7.0 (d,1), 6.75 (d,1), 2.4 (s,3), 2.2 (s,3) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl(oxy]benzonitrile;

3-[(3,5-difluoro-6-(3-(2-(dimethylamino)ethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile;

1-[3-((6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy)phenyl]urea;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoic acid, ethyl ester;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzenecarboxamide;

3-[(3,5-difluoro-6-(3-ethylaminophenoxyl-4-methylpyridin-2-yl)oxy]benzonitrile;

3-[(6-(3-diethylaminophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile;

3[(3,5-difluoro-4-methyl-6-(3-phenylaminophenoxylpyridin-2-yl)oxy]benzonitrile;

3-[(6-(3-chlorophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.4 (m,2), 7.2-7.33 (m,3), 7.13 (ddd,1), 7.0 (t,1), 6.91 (ddd,1), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-trifluoromethylphenoxy)pyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.42 (m,3), 7.33 (t,1), 7.15-7.3 (m,4), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-13-methoxyphenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.25-7.42 (m,5), 6.72 (ddd,1), 6.6 (m,1), 6.58 (m,1), 3.8 (s,3), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-fluorophenoxy)-4-methylpyridin-2-yl)oxy]benzonitrile; NMR (CDCl₃) 7.35-7.45 (m,2), 7.2-7.33, (m,3), 6:85 (m,2), 6.73 (dt,1), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-4-methylbenzonitrile; NMR (CDCl₃) 7.28 (m,1), 7.26 (s,1), 7.2 (m,2), 7.12 (t,1), 6.48 (dd,1), 6.28 (m,2), 2.88 (s,6), 2.38 (s,3), 2.21 (s,3) ppm;

4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)-oxy]benzonitrile; NMR (CDCl₃) 7.2 (m,3), 6.66 (d,1), 6.54 (d,1), 6.35 (m,2), 4.28 (s,2), 2.91 (s,6), 2.37 (s,3) ppm;

3-[(6-(5-cyano-2-methoxyphenoxy)pyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (CDCl₃) 7.7 (t,1), 7.4 (dd,1), 7.3 (d,1), 7.27 (d,1), 7.15 (dt,1), 7.0 (m,2), 6.9 (d,1), 6.66 (d,1), 6.57 (d,1), 3.8 (s,3), 3.1 (s,3), 2.9 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-hydroxybenzoic acid, ethyl ester; NMR (CDCl₃) 7.3 (m,6), 6.7 (s,1), 4.3 (q,2), 2.4 (s,3), 1.5 (t,3) ppm;

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-hydroxybenzoic acid; NMR (CDCl₃) 7.4 (d,1), 7.3 (m,2), 7.1 (s,1), 6.8 (d,1), 6.6 (s,1), 5.6 (s,1), 4.4 (q,2), 3.8 (s,3), 2.4 (s,3), 1.4 (t,3) ppm;

2-(3-cyanophenoxy)-6-(5-cyano-2-(benzyloxy)phenoxy)pyridine-4-carboxylic acid, ethyl ester; NMR (CDCl₃) 7.62-7.02 (m,12), 5.16 (s,2H), 4.42 (q,2), 1.41 (t,3) ppm;

N-[2-(5-cyano-2-methoxyphenoxy)-6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoropyridin-4-yl]-N-methylglycine, ethyl ester;

N-[2-(5-cyanophenoxy)-6-(3-dimethylaminophenoxy)-3,5-difluoropyridin-4-yl]-N-methylglycine, ethyl ester;

3-[(6-(5-cyano-2-benzyloxyphenoxy)-3,5 difluoro-4-(morpholin-1-yl)pyridin-2-yl)oxy]-N,N-dimethylbenzamide;

2-(5-cyano-2-methoxyphenoxy)-6-(3-dimethylaminocarbonylphenoxy)pyridine-4-carboxylic acid, methyl ester; NMR (CDCl₃) 7.2 (m,9), 3.92 (s,3), 3.70 (s,3), 3.10 (s,3), 2.88 (s,3) ppm;

2-(5-cyano-2-methoxyphenoxy)-6-(3-dimethylaminocarbonylphenoxy)-N,N-dimethylpyridine-4-carboxamide; NMR (CDCl₃) 7.1 (m,7), 6.55 (s,1), 6.48 (s,1), 3.65 (s,3), 2.95 (m,12) ppm;

2-(3-cyanophenoxy)-6-(3-dimethylaminocarbonylphenoxy)-N,N-dimethylpyridine-4-carboxamide; NMR (CDCl₃) 7.16 (m,8), 6.57 (s,1), 6.53 (s,1), 2.95 (m,12) ppm; and

4-[(2-(3-aminophenoxy)-6-(5-cyano-2-phenylmethoxyphenoxy)-3,5-difluoropyridin-4-yl)oxy]-3-methoxybenzoic acid, ethyl ester.

PREPARATION 10

2,6-Bis(3-cyanophenoxy)-N-methylpyridine-4-carboxamide

[0100] 

A. To 2,6-bis(3-cyanophenoxy)pyridine-4-carboxylic acid, ethyl ester (1.6 g, 4.0 mmol) in tetrahydrofuran/water (50 mL, 1/1) was added lithium hydroxide (0.85 g, 20 mmol). After stirring for 1.5 hours the reaction was partitioned with 1 M HCI and ethyl acetate. The organic layer was separated, dried (MgSO₄), and the solvent was removed in vacuo. The residue was dissolved in methylene chloride (50 mL) and thionyl chloride (2.4 g, 20 mmol) was added. After stirring for 2 hours the solvent was removed in vacuo. The residue was dissolved in methylene chloride/water (30/10 mL) and methylamine hydrochloride (0.090 g, 1.3 mmol) and potassium carbonate (0.46 g, 3.3 mmol) were added. The organic layer was separated, washed with brine, dried (MgSO₄), and the solvent removed in vacuo to give 2,6-bis(3-cyanophenoxy)-N-methylpyridine-4-carboxamide; NMR (CDCl₃) 7.5 (m,4), 7.3 (m,4), 7.0 (s,2), 6.25 (br s,1), 3.1 (d,3) ppm.

B. In a similar manner, the following compounds were made:

2,6-bis (3-cyanophenoxy)-N-methylpyridine-3-carboxamide; NMP CCDCl₃) 7.8 (d,1), 7.4-7.6 (m,5), 7.1-7.3 (m,4), 6.8 (d,1), 3.1 (d,3) ppm;

N-[(2,6-bis (3-cyanophenoxy)pyridin-3-yl)oxomethyl]glycine, ethyl ester; NMR (CDCl₃) 8.65 (d,1), 8.1 (t,1), 7.2-7.6 (m,8), 6.8 (d,1), 4.3 (m,4), 1.3 (t,3) ppm; and

2,6-bis(3-cyanophenoxy)-N,N-dimethylpyridine-4-carboxamide; NMR (CDCl₃) 7.85 (d,1), 7.45 (m,4), 7.25 (m,4), 6.75 (d,1), 3.2 (s,3), 3.1 (s,3) ppm.

PREPARATION 11

3-[(6-(3-Cyanophenyl)methylamino-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzonitrile

[0101] 

A. To 3-[(6-(3-cyanophenyl)amino-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzonitrile (0.10 g, 0.28 mmol) in acetonitrile (10 mL) was added iodomethane (0.20 g, 1.4 mmol) and sodium hydride (0.055 g, 1.4 mmol). After stirring for 18 hours the reaction was partitioned with water and ethyl acetate. The organic layer was separated, dried (Na₂SO₄), and the solvent was removed in vacuo. Chromatography of the residue on silica gel with ethyl acetate/hexane (1/3) as eluent gave 3-[(6-(3-cyanophenyl)-methylamino-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzonitrile;NMR (CDCl₃) 7.4 (m,5), 7.25 (m.1), 7.1 (m,2), 3.25 (s,3), 2.3 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3-(4-methyl-3,5,6-trifluoropyridin-2-yl)methylaminobenzonitrile; NMR (CDCl₃) 7.35 (t,1), 7.3 (m,1), 7.2 (m,2), 3.4 (s,3), 2.3 (s,3) ppm; and

3,3'-[3,5-difluoro-4-methyl-2,6-pyridinediylbis(methylamino)]bis(benzonitrile); NMR (CDCl₃) 7.1-7.5 (m,8), 3.4 (s,6), 2.3 (s,3) ppm.

PREPARATION 12

3-[(6-(3-Cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-methoxybenzoic Acid, Ethyl Ester

[0102] 

A. To acetonitriie (5 mL) was added 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-hydroxybenzoic acid, ethyl ester (0.20 g, 0.47 mmol), cesium carbonate (0.31 g, 0.94 mmol), and iodomethane (0.13 g, 0.94 mmol). After stirring for 15 hours the mixture was partitioned with ethyl acetate and water. The organic layer was dried (MgSO₄) and the solvent was removed in vacuo to give 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methyl-pyridin-2-yl)oxy)-5-methoxybenzoic acid, ethyl ester; NMR (CDCl₃) 7.3 (m,6), 6.8 (s,1), 4.4 (q,2), 3.8 (s,3), 2.4 (s,3), 1.4 (t,3) ppm.

B. In a similar manner, the following compound was made:

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-methoxybenzoic acid, ethyl ester; NMR (CDCI₃) 7.4 (d,1), 7.3 (m,2), 7.1 (s,1), 6.8 (d,1), 6.6 (s,1), 4.4 (q,2), 3.8 (s,3), 3.7 (s,3), 2.4 (s,3), 1.4 (t,3) ppm.

PREPARATION 13

5-[(6-(3-Cyanophenoxyl-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene1,3-dicarboxylic acid

[0103] 

A. To 5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-1,3-dicarboxylic acid, diethyl ester (0.97 g, 2.0 mmol) in tetrahydrofuran/water (20 mL, 1/1) was added lithium hydroxide (0.42 g, 10 mmol). After heating at 60°C for 90 minutes, the material was partitioned between ethyl acetate and 2 N HCl. The organic layer was separated, dried (MgSO₄), and the solvent removed in vacuo to give 5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-1,3-dicarboxylic acid; NMR (DMSO) 8.25 (s,1), 7.85 (s,2), 7.4-7.7 (m,3), 7.3 (m,3), 2.4 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-2,3-dimethoxybenzenecarboxylic acid; NMR (DMSO-d₆) 7.95 (s,1), 7.1-7.7 (m,5), 3.85 (s,3), 3.6 (s,3), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-methoxybenzoic acid; and

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-5-methoxybenzoic acid.

PREPARATION 14

3-[(6-(3-Cyanophenoxyi-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethyl-4-methoxybenzamide

[0104] 

A. To 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-4-methoxybenzoic acid (0.47 g, 1.1 mmol) in tetrahydrofuran (12 mL) was added 1,1'-carbonyldiimidazole (0.22 g, 1.4 mmol) and stirred at ambient temperature for 3 hours. Then dimethylamine (aq, 0.077 g, 1.7 mmol) was added. After stirring for 12 hours the solution was partitioned between water and ethyl acetate. The organic layer was separated, dried (MgSO₄), and the solvent was removed in vacuo. Chromatography on silica gel with ethyl acetate/hexane (1/8) as eluent gave 3-[(6-(3-cyanophenoxy)3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethyl-4-methoxybenzamide; NMR (CDCl₃) 6.9-7.4 (m,7), 3.8 (s,3), 3.0 (br,6), 2.4 (s,3) ppm.

B. In a similar manner, the following compounds were made:

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethyl-4-methoxybenzamide; NMR (CDCl₃) 7.3 (m,2), 7.2 (m,3), 7.15 (d,1), 6.95 (s,1), 3.05 (br,3), 2.85 (br,3), 2.4 (s,3), 2.15 (s,3) ppm;

5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N,N',N'-tetraethylbenzene-1,3-dicarboxamide; NMR (CDCl₃) 7.9 (s,1), 7.65 (s,2), 7.1-7.5 (m,4), 3.45 (br,4), 3.15 (br,4), 2.4 (s,3), 1.25 (br,6), 1.05 (br,6) ppm;

5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-2,3-dimethoxy-N,N-dimethylbenzamide; NMR (DMSO-d₆) 7.95 (m,1), 7.1-7.7 (m,5), 3.9 (s,3). 3.65 (s,3), 3.4 (s,3), 3.15 (s,3), 2.4 (s,3) ppm;

5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N,N',N'-tetramethylbenzene-1,3-dicarboxamide; NMR (CDCIg) 7.7 (s,2), 7.1-7.5 (m,5), 3.1 (m,6), 2.9 (s,3), 2.85 (s,3), 2.4 (s,3) ppm;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-3-methoxy-N,N-dimethylbenzamide; NMR (CDCl₃) 7.7 (s,1), 7.2-7.4 (m,3), 7.1 (s,1), 7.05 (m,1), 6.95 (d,1), 3.8 (5,3), 3.1 (s,3), 3.0 (s,3), 2.4 (s,3) ppm;

1-[3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoyl]pyrrolidine; NMR (CDCI3) 7.2-7.5 (m,6), 7.2 (s,1), 7.1 (d,1), 3.65 (m,2), 3.3 (m,2), 2.4 (s,3), 1.8-2.1 (m,4) ppm;

1-[3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoyl]morpholine;

4-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethylbenzamide; NMR (COCI3) 7.2-7.6 (m,6), 7.05 (d,2), 3.2 (br,3), 3.0 (br,3), 2.4 (s,3) ppm;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N-methylbenzenecarboxamide;

1-[3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoyl]-4-ethylpiperazine;

1-13-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoyl]piperidine;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N-methyl-N-(phenylmethyl) benzamide; .

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N-methyl-N-[2-(pyridin-2-yl)ethyl]benzamide;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N-ethyl-N-methylbenzamide;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-diethylbenzamide;

N-[3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzoyl]-β-alanine, ethyl ester;

3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethyl-5-methoxybenzamide; NMR (CDCl₃) 7.4 (m,2), 7.3 (m,2), 6.7 (s,1), 6.6 (s,2), 3.8 (s,3), 3.0 (s,3), 2.8 (s,3), 2.4 (s,3) ppm; and

3-[(6-(5-cyano-2-methoxyphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-N,N-dimethyl-5-methoxybenzamide; NMR (CDCl₃) 7.4 (d,1), 7.3(s,1), 6.9 (d,1), 6.6 (d,1), 6.5 (d,1), 3.8 (s,6), 3.1 (s,3), 2.9 (s,3), 2.4 (s.3) ppm.

PREPARATION 15

[0105] 3,3'-[3-Amino-2,6-pyridinediylbis(oxy)]bis(benzonitrile)

A. To 3,3'-[3-nitro-2,6-pyridinediylbis(oxy)]bis(benzonitrite) (18.5 g, 50 mmol) dissolved in ethanol/ethyl acetate (500 mL, 2/3) was added 10% palladium on carbon (1.8 g). After subjecting the mixture to hydrogen at 1.03·10⁵ Pa for 2 hours, the reaction was suction filtered through celite®. The solvent was removed in vacuo to give 3,3'-[3-amino-2,6-pyridinediylbisloxy)]-bis(benzonitrile); NMR (CDCI₃) 7.5 (m,7), 7.2 (m,2), 6.6 (d,1). 3.8 (br,2) ppm.

PREPARATION 16

N-[2,6-Bis(3-cyanophenoxy)pyridin-3-yl]benzamide

[0106] 

A. To 3,3'-[3-amino-2,6-pyridinediylbis(oxy)]bis(benzonitrile) (1.0g,2.9 mmol) dissolved in acetonitrile (50 mL) was added benzoyl chloride (0.50 g, 3.5 mmol) and triethylamine (0.45 g, 0.60 mmol). After stirring for 3 hours, the reaction was partitioned between ether and water. The organic layer was separated, washed with water, saturated aqueous sodium bicarbonate, and brine, dried (MgSO₄), and the solvent was removed in vacuo. Chromatography on silica gel with ethyl acetate/hexane(1/3) as eluent gave N-[2,6-bis(3-cyanophenoxy)-pyridin-3-yl]benzamide; NMR (CDCl₃) 8.95 (d,1), 8.25 (s,1), 7.9 (d,1). 7.2-7.7 (m,12), 6.8 (d,1) ppm.

B. In a similar manner, the following compounds were made:

N-[2,6-bis(3-cyanophenoxy)pyridin-3-yl]acetamide; NMR (CDCl₃) 8.65 (d,1). 7.6 (s,1), 7.1-7.6 (m,8), 6.7 (d,1), 2.3 (s,3) ppm;

N-[[(2,6-bis(3-cyanophenoxy)pyridin-3-yl)amino]carboxylglycine, ethyl ester; NMR (CDCI₃) 8.5 (d,1), 7.2-7.5 (m,8), 7.15 (s,1), 6.6 (d,1), 5.7 (m,1), 4.2 (q,2), 4.1 (m,2), 1.25 (d,3) ppm;

N-[2,6-bis(3-cyanophenoxy)pyridin-3-yl]methanesulfonamide; NMR (CDCI₃) 8.0 (d,1), 7.45 (m,4), 7.25 (m.4), 6.75 (d,1), 6.6 (s,1), 3.1 (s,3) ppm; and

N-[3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]phenyl]methanesulfonamide; NMR (CDCI₃) 8.8 (d,1), 7.65 (m,2), 7.35 (m,4), 7.05 (m,2), 2.95 (s,3). 2.3 (s,3) ppm.

PREPARATION 17

N-[2,6-Bis(3-cyanophenoxy)pyridin-3-yl]-N'-phenylurea

[0107] 

A. To 3,3'-[3-amino-2,6-pyridinediylbis(oxy)]bis(benzonitrile) (3.0g,8.7 mmol) dissolved in acetonitrile (100 mL) was added phenyl isocyanate (1.1 g, 9.5 mmol). After refluxing for 4 hours, the reaction was partitioned between ether and water. The organic layer was separated, washed with water, saturated aqueous sodium bicarbonate, and brine, dried (MgSO₄), and the solvent was removed in vacuo. Chromatography on silica gel with ethyl acetate/hexane (1/4) as eluent gave material which was crystallized from ethyl acetate/hexane to give N-[2,6-bis(3-cyano-phenoxy)pyridin-3-yl]-N'-phenylurea; NMR (CDCl₃) 8.65 (d,1), 7.4 (m,8), 7.1-7.3 (m,6), 6.8 (s,1), 6.7 (d,1) ppm.

B. In a similar manner, the following compound was made:

N-[2,6-bis(3-cyanophenoxy)pyridin-3-yl]-N'-methylurea; NMR (CDCl₃) 8.65 (d,1), 7.5 (m,4), 7.25 (m,4), 6.8 (s,1), 6.7 (d,1), 2.9 (d,3) ppm.

PREPARATION 18

3-[(6-(3-Cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzenepropionic Acid, Methyl Ester

[0108] To 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-propionicacid(0.50 g, 1.2 mmol) in methylene chloride (20 mL) was added methyl iodide (0.26 g, 1.8 mmol) and diazabicycloundecane (2.8 g, 1.8 mmol). After stirring for 15 hours, the solution was concentrated in vacuo and chromatographed on silica gel with ethyl acetate/hexane (1/4) to give 3-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzenepropionic acid, methyl ester; NMR (CDCl₃) 7.3 (m,5), 7.05 (d,1), 6.85 (m,2), 3.68 (s,3), 2.9 (t,2), 2.55 (t,2), 2.4 (s,3) ppm.

PREPARATION 19

4,4'-[1,3-Phenylenebis(oxy)]benzonitrile

[0109] To DMSO (6 mL) was added resorcinol (1.1 g, 10 mmol), 4-fluorobenzonitrile (2.4 g, 20 mmol) and potassium carbonate (2.4 g, 17 mmol). After heating in an oil bath at 100°C for 16 hours the reaction mixture was partitioned with water and ethyl acetate. The organic layer was separated, washed with 1 N sodium hydroxide, water, brine, dried (sodium sulfate) and concentrated in vacuo. Chromatography on silica gel with methylene chloride/hexane (20/1) as eluent gave 4,4'-[1,3-phenylenebis(oxyl)]benzonitrile; NMR (CDCl₃) 7.64 (d,4), 7.43 (t,1), 7.06 (d,4), 6.82 (dd,2), 6.80 (t,1) ppm.

PREPARATION 20

4_-[(2-[3-(Guanidine)phenoxy)-6-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoropyridin-4-yl)oxy]-3-methoxybenzoic Acid, Ethyl Ester.

[0110] To ethanol (15 mL) was added 4-[[2-(3-aminophenoxy)-6-(5-cyano-2-phenylmethoxyphenoxy)-3,5-difluoropyridin-4-yl]oxy]-3-methoxybenzoic acid, ethyl ester (0.50 g, 0.80 mmol), cyanamide (0.60 g, 14 mmol), and 6 M hydrochloric acid (0.7 mL). After refluxing for 19 hours, cyanamide (0.60 g, 14 mmol) and 6 M hydrochloric acid (0.7 mL) was added and refluxing was continued for 4 hours. The reaction mixture was concentrated in vacuo and purified by HPLC to give 4-[[2-(3-(guanidino)phenoxy)-6-(5-cyano-2-benzyloxyphenoxy)-3,5-difluoropyridin-4-yl)oxy]-3-methoxybenzoic acid, ethyl ester.

EXAMPLE 1

3,3'-[2,6-Pyridinediylbis(oxy)]bis(benzamidine), Dihydrochloride

[0111] 

A. To 3,3'-[2,6-pyridinylbis(oxy)]bis(benzonitrile) (0.2 g, 0.7 mmol) slurried in ethanol (6 mL) cooled in a dry ice/isopropanol bath was bubbled HCI (g). After the solution was saturated the reaction flask was sealed and allowed to warm to ambient temperature and stir for 18 hours. The solvent was removed in vacuo and the residue was triturated with ether. The ether was removed by decantation and the residue was dissolved in ethanol (6 mL). The solution was cooled in a dry ice/isopropanol bath and ammonia (g) was bubbled in. The reaction flask was sealed and heated to 50°C for 2 hours. The solvent was removed in vacuo and the residue was recrystallized from 5 M HCI to give 3,3'-[2,6-pyridinediylbis(oxy)]bis(benzamidine), dihydrochloride as a solid; m.p. 160°C (decom); NMR (DMSO-d₆) 9.45 (s,4), 9.3 (s,4), 8.02 (t,1), 7.4-7.8 (m,8), 6.90 (d,2) ppm.

B. In a similar manner, the following compounds were made:

4,4'-[2,6-pyridinediylbis(oxy)]bis(benzamidine), dihydrochloride; NMR (DMSO-d₆) 9.4 (s,4), 9.2 (s,4), 8.1 (t,1), 7.95 (d,4), 7.40 (d,4), 6.96 (d,2) ppm;

3,3'-bis(methoxy)-4,4'-(2,6-pyridinediybis(oxy)]bis(benzamidine), dihydrochloride; NMR (DMSO-d₆) 9.5 (br s,4), 9.2 (br s,4), 7.9 (t,1), 7.7 (s,2), 7.5 (d,2), 7.3 (d,2), 6.7 (d,2), 3.85 (s,6) ppm;

4-[(6-(3-amidinophenoxy)pyridin-2-yl)oxy]-3-methoxybenzamidine, dihydrochloride; NMR (DMSO-d₆) 9.7 (s,2), 9.55 (s,2), 9.4 (brs,4), 7.95 (t,1), 7.75 (s,1), 7.3-7.7 (m,6), 6.85 (d, 1), 6.75 (d,1), 3.9 (s,3) ppm;

3-[(3,5-difluoro-6-(3-ethylamino-4-methylphenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, dihydrochloride; NMR (DMSO-dg) 9.4 (s,2), 9.2 (s,2), 7.6 (m,2), 7.55 (t,1), 7.45 (m,1), 7.3 (m,2), 7.15 (dd,1), 3.2 (q,2), 2.4 (s,3), 2.35 (s,3), 1.2 (t,3) ppm;

3,3'-[3-trifluoromethyl-2.6-pyridinediylbis(oxy)]bis(benzamidine), dihydrochloride; NMR (DMSO-d₆) 9.4 (s,4), 9.2 (s,4), 8.3 (d,1), 7.7 (m,4), 7.6 (d,4), 7.0 (m,1) ppm;

3,4'-[2,6-pyridinediylbis(oxy)]bis(benzamidine), dihydrochloride; NMR (DMSO-d₆) 9.4 (br s,8), 8.1 (t,1), 7.9 (d,2), 7.5-7.8 (m,4), 7.40 (d,2), 6.95 (m,2) ppm;

3,3'-(3-methylaminocarbonylamino-2,6-pyridinediylbis(oxy)]bis(benzamidine), dihydrochloride; m.p. 205-206°C;

4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-carboxypyridin-2-yl)oxy]benzamidine, hydrochloride; NMR (DMSO-d₆) 9.2 (s,2l, 9.0 (s,2), 7.9 (t,1), 7 78 (dd,1), 7.68 (m,1), 7.36 (t,1), 7.26 (d,1), 7.15 (d,1), 7.05 (m,1), 7.02 (m,1), 6.75 (d.1), 6.7 (d,1), 3.8(s,3), 2.95(s,3), 2.8 (s,3) ppm;

4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-methylpiperazinoyl)pyridin-2-yl)oxy]benzamidine, dihydrochloride;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)(ethoxycarbonylmethyl)amino) pyridin-2-yl)oxy]benzamidine, ethyl ester, hydrochloride; NMR (DMSO-dg) 9.3 (s/2), 9.2 (s,2), 7.5 (m,4), 7.2 It,1), 6.7 (m,2), 6.5 (d,1), 4.2 (s,2), 3.2 (s,3), 2.9 (s,6) ppm;

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(dimethylaminocarbonyl)pyridin-2-yl)oxy]benzamidine, hydrochloride;

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonyl)-pyridin-2-yl)oxy]benzamidine, hydrochloride; and

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(ethoxycarbonyl)pyridin-2-yl)oxy]benzamidine, hydrochloride.

C. In a similar manner, reaction of 3,3'-[3,5-difluoro-4-methyl-2,6-pyridinediylbis(oxy)]bis(benzonitrile) gave 3,3'-[3,5-difluoro-4-methyl-2,6-pyridinediylbis(oxy)]bis(benzamidine); which was purified by HPLC on a C18 Dynamax column with a 20-80% acetonitrile in water gradient with 0.1 % trifluoroacetic acid to give the compound as a pure trifluoroacetic acid salt; m.p. > 210°C; NMR (DMSO-d₆) 9.3 (br s,8), 7.5 (m,4), 7.54 (m,4), 2.4 (m,3) ppm.

D. In a similar manner, the following compounds were made:

3,3'-(3,5-dichloro-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.2 (br s,8), 8.6 (s,1), 7.4-7.7 (m,8) ppm;

4,4'-(3,5-dichloro-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.25 (s,4), 9.0 (s,4), 8.58 (s,1), 7.8 (d,4) 7.4 (d,4) ppm;

3,3'-(4-ethoxycarbonyl-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.55 (br s,4), 9.4 (br s,4), 7.65 (m,4), 7.6 (m,4), 7.2 (s,2), 4.4 (q,2), 1.4 (t,3) ppm;

3,3'-(3-ethoxycarbonyl-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (br s,4), 9.1 (br s,4), 8.4 (d.1), 7.6 (m,4), 7.5 (m,4), 6.9 (d,1), 4.3 (q,2), 1.3 (t,3) ppm;

3,3'-(3,5-difluoro-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.55 (br s,4), 9.4 (br s,4), 8.5 (t,1), 7.7 (m,4), 7.55 (m,4) ppm;

3,3'-(4-methylaminocarbonyl-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (br s,4), 9.2 (br s,4), 8.85 (m,1), 7.5-7.7 (m,8), 7.2 (s,2), 2.9 (d,3) ppm;

3,3'-(3-methylaminocarbonyl-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.6 (m,4), 9.4 (br s,4), 8.65 (d,1). 8.5 (m,1), 7.7-8.0 (m,8), 7.2 (d,1), 2.85 (d,3) ppm.

3,3'-(3-dimethylaminocarbonyl-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; m.p. 180-183°C;

3,3'-(3-((aminocarbonyl)methylaminocarbonyl)-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.25 (s,2), 9.05 (s,4), 8.5 (d.1), 7.4-7.7 (m,11), 6.85 (d,1), 4.0 (d,2) ppm;

3-[(3,5-difluoro-6-(5-dimethylamino-2-methylphenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.25 (s,2), 9.1 (s,2), 7.4-7.6 (m,3), 7.2-7.4 (m,4), 3.1 (s,6), 2.4 (s,3), 2.1 (s,3) ppm;

3-[(3,5-difluoro-6-(3-dimethylamino-2-methylphenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.25 (s,2), 9.1 (s,2), 7.5-7.7 (m,4), 7.4 (m,1), 7.3 (m,1), 7.2 (d,1), 3.1 (s,6), 2.4 (s,3), 2.3 (s,3) ppm;

3-[(3,5-difluoro-6-[(3-amidinophenyl)methylamino)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (s,2), 9.3 (s,2), 9.15 (s,2), 9.05 (s,2), 7.6 (m,4), 7.4 (m,3), 7.25 (m,1), 7.2 (d,1), 3.25 (s,3), 2.3 (s,3) ppm;

3-[(3,5-difluoro-6-[(3-amidinophenyl)amino]-4-methylpyridin-2-yl)oxy]-benzamidine; trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (s,2), 9.2 (s,4), 8.95 (s,2), 7.5-7.8 (m,6), 7.25 (m,2), 2.35 (s,3) ppm;

3,3'-(3,5-difluoro-4-methoxy-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (br s,4), 9.2 (br s,4), 7.6 (m,4), 7.5 (m,4), 4.3 (s,3), 2.3 (m,3) ppm;

3,3'-(3,5-difluoro-4-methyl-2,6-pyridinediylbis(methylamino))bis(benzamidine), trifluoroacetic acid salt; m.p. 115-120°C;

3-[(6-(2-methoxy-5-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.1 (s,2), 7.5 (m,3), 7.3 (d,1), 7.2 (m,2), 7.1 (d,1), 3.75 (s,3). 2.9 (br,6), 2.4 (s,3) ppm;

3-[(6-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; m.p. 200-202°C;

3-[(6-(2-methyl-5-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.15 (s,2), 7.5 (m,3), 7.45 (d,1), 7.3 (d,1), 7.1 (m,2), 2.95 (s,3), 2.75 (s,3), 2.4 (s,3), 2.15 (s,3) ppm;

3-[(6-(3,5-di(diethylaminocarbonyl)phenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (s,2), 9.05 (s.2), 7.6 (m,3), 7.45 (m,1), 7.2 (s,2), 7.1 (s,1), 3.45 (br,4), 3.15 (br,4), 2.4 (s,3) 1.2 (br,6), 1.05 (br,6) ppm;

3-[(6-(2,3-dimethoxy-5-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.25 (s,2), 9.1 (s,2), 7.95 (s,1), 7.4-7.6 (m,4), 7.3 (s,1), 3.9 (s,3), 3.7 (s,3), 2.5 (s,6), 2.4 (s,3) ppm;

3-[(6-(3,5-di(dimethylaminocarbonyl)phenoxy)-3,5-difluoro-4-methylpyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.05 (s,2), 7.55 (m,4), 7.25 (s,2), 7.2 (s,1), 3.0 (s,6), 2.85 (s,6), 2.4 (s,3) ppm;

3-[(6-(2-methoxy-4-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.15 (s,2), 7.5 (m,3), 7.35 (m,1), 7.15 (d,1), 7.1 (s,1), 6.9 (d,1), 3.7 (s,3), 3.05 (br,3), 2.9 (br,3), 2.4 (s,3) ppm;

3,3'-(4-phenylcarbonylamino-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; m.p. 269-271 °C;

3,3'-(3-phenylaminocarbonylamino-2,6-pyridinediylbis(oxy))bis(benzamidine), trifluoroacetic acid salt; m.p. 159-160°C;

3,3'-(3-(aminocarbonylmethyl)aminocarbonylamino-2,6-pyridinediylbis(oxy))-bis(benzamidine), trifluoroacetic acid salt; m.p. 129-130°C;

3,3'-[3-amino-2,6-pyridinediylbis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.5 (br,4), 9.2 (br,4), 7.3-7.7 (m,9), 6.8 (d,1) ppm;

3,3'-[3-methylsulfonylamino-2,6-pyridinediylbis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.6 (s,1), 9.4 (m,8), 8.4 (d,1), 7.95 (d,1), 7.5-7.7 (m,8), 6.9 (d,1), 3.1 (s.3) ppm;

3,3'-[3-methylcarbonylamino-2,6-pyridinediylbis(oxy)]bis(benzamidine), 2-trifluoroacetic acid salt; NMR (DMSO-d₆) 9.8 (s,1), 9.3 (m,4), 9.25 (m,4), 8.4 (d,1), 7.4-7.7 (m,8), 6.9 (d,1), 2.15 (s,3) ppm;

3-[(6-(3-aminophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.35 (s,2), 9.2 (s,2), 7.6 (m,3), 7.55 (m,1), 7.0 (t,1), 6.45 (d,1), 6.35 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-[3-[2-(1H-imidazol-1-yl)-1-oxoethyl)phenoxyl-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (s,2), 9.3 (s.2), 9.0 (s,1), 7.4-7.9 (m,10), 6.0 (s.2), 2.4 (s,3) ppm;

3-[(6-(3-(2-(dimethylaminocarbonyl)ethyl)phenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.25 (s,2), 7.6 (m,4), 7.2 (t,1), 7.0 (m,2), 6.9 (d,1), 2.9 (s,3), 2.8 (s,3), 2.75 (t,2), 2.5 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-[3-(hydroxymethyl)phenoxy]-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (br,4), 7.6 (m,4), 7.25 (t,1), 7.1 (d,1), 7.05 (m,1), 7.0 (d,1), 4.45 (s,2), 2.4 (s,3) ppm;

3-[(6-(3-(dimethylaminocarbonyl)methylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,4), 7.6 (m,3), 7.55 (m,1), 7.2 (t,1), 7.0 (m,2), 3.6 (s,2), 2.95 (s,3), 2.8 (s,3), 2.4 (s,3) ppm;

3-[(6-(3-laminocarbonyl)methylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; m.p. 189-192°C;

3-[(6-[3-(aminomethyl(phenoxy]-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (br,4), 8.2 (br,3), 7.6 (m,3), 7.55 (m.1), 7.35 (t,1), 7.2 (m,2), 7.15 (d,1), 4.0 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-[3-(prop-2-oxymethyl)phenoxy]pyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.1 (s,2), 7.6 (m,4), 7.2 (t,1), 6.65 (m,3), 4.55 (m,1), 2.4 (s,3), 1.15 (m,6) ppm;

4,4'-[1,3-phenylenebis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (br,4), 9.2 (br,4), 7.96 (d,4), 7.6 (t,1), 7.3 (d,4), 7.05 (dd,2), 6.97 (m,1) ppm;

3,3'-[4-nitro-1,3-phenylenebis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (s,4), 9.2 (m,4), 8.25 (d,1), 7.6 (m,8), 7.0 (dd,1), 6.9 (m,1) ppm;

3-[(6-(3-methoxy-5-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.1 (s,2), 7.6 (m,4), 6.8 (s,1), 6.7 (d,2), 3.7 (s,3), 3.0 (s,3), 2.8 (s,3), 2.4 (s,3) ppm;

4-methoxy-3-[(6-(3-methoxy-5-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.1 (s,2), 9.0 (s,2), 7.8 (d,1), 7.7 (s,1), 7.2 (d,1), 6.7 (s,1), 6.6 (s,1), 6.5 (s,1), 3.8 (s,3), 3.7 (s,3), 2.9 (s,3), 2.7 (s,3), 2.4 (s,3) ppm;

4-methoxy-3-[(6-(3-(imidazol-1-yl)phenoxy)-4-ethoxycarbonylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.1 (s,2), 8.9 (s,2), 8.0 (s,1), 7.6 (m,7), 7.2 (m,4), 4.4 (q,2), 3.7 (s,3), 1.3 (t,3) ppm;

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt, NMR (CDCl₃) 9.10 (s,2), 8.94 (s,2), 7.71 (d,1), 7.66 (s,1), 7.32 (t,1), 7.25 (d,1), 7.09 (d,1), 7.01 (d,1), 6.95 (s,1), 3.77 (s,3), 2.95 (s,3), 2.75 (s,3), 2.37 (s,3);

4-amino-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzamidine, trifluoroacetic acid salt; NMR (CDCl₃) 8.8 (s,4), 7.71 (d,1), 7.5 (d,1), 7.4 (s,1), 7.3 (t,1), 7.1-7.2 (m,2), 7.1 (s,1), 6.6 (d,1), 6.2 (s,2), 3.0 (s,3), 2.8 (s,3), 2.4 (s,3) ppm;

4-amino-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-(2,2,2-trifluoroethoxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CDCl₃) 8.7 (s,2), 8.5 (s,2), 7.4-7.5 (m,2), 7.3 (t,1), 7.1-7.2 (m,3), 6.7 (d,1), 6.2 (br s,2), 5.2 (q,2), 3.0 (s,3), 2.8 (s,3) ppm;

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

3,3'-[2,6-pyrazinediylbis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (s,8), 8.4 (s,2), 7.6 (m,8) ppm;

3,3'-[2,6-pyrimidinediylbis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO-d₆) 9.4 (m,8), 8.6 (d,1), 7.7 (m,8), 7.05 (d,1) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-2-methoxypyridin-4-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.3 (s,1), 9.1 (m,2), 8.8 (s,2), 7.6 (m,2), 7.5 (t,1), 7.2 (m,3). 7.05 (d,1), 3.8 (s,3), 3.0 (s,3), 2.9 (s,3) ppm;

4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-(aminocarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(methyl)-(phenyl)aminocarbonylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-methoxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-3,5-difluoro-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

3-[(6-(3-dimethylaminocarbonylprienoxy)-4-dimethylaminocarbonylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.31 (s,2), 9.24 (s,2), 7.35 (m,8), 6.81 (s,1), 6.78 (s,1), 2.95 (m,12) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonyl-2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonyl-2-(morpholin-4-ylmethy))phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

3-[(3-(3-amidinophenoxy)phen-1-yl]oxy]benzamidine, trifluoroacetic acid salt.

EXAMPLE 2

3-[(6-(3-Amidinophenoxy)-4-carboxypyridin-2-yl)oxy]benzamidine, Dihydrochloride

[0112] 2,6-Bis(3-amidinophenoxy)pyridine-4-carboxamide (5 g, 11 mmol) was dissolved in 5 M HCI and heated. The solid that precipitated on cooling was collected by filtration to give 3-[(6-(3-amidinophenoxy)-4-carboxypyridin-2-yl)oxy]benzamidine, dihydrochloride; NMR (DMSO-d₆) 9.4 (br s,4), 9.2 (br s,4), 7.4 (m,4), 7.3 (m,4), 7.2 (s,2) ppm.

EXAMPLE 3

3-[(3,5-Difluoro-4-methyl-6-[(pyridin-3-yl)oxy)pyridin-2-yl)oxy]benzamidine, Acetic Acid Salt

[0113] 

A. In a manner similar to Example 1 above, 3-[(3,5-difluoro-4-methyl-6-[(pyridin-3-yl)oxy]pyridin-2-y]oxy]benzonitrile was reacted with HCI and ammonia (g). The solvent was removed in vacuo and the material was partitioned with methylene chloride and 2 N aqueous potassium hydroxide. The organic layer was separated, acetic acid added, and the solvent was removed in vacuo. The residue was triturated with ether and the resulting solid was filtered to give 3-[(3,5-difluoro-4-methyl-6-[(pyridin-3-yl)-oxy]pyridin-2-yl)-oxy]benzamidine, acetic acid salt; m.p. 213-214°C.

B. In a similar manner, the following compounds were made:

3-[(3,5-difluoro-4-methyl-6-phenoxypyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 122-123°C;

3-[(3,5-difluoro-6-(4-dimethylaminophenoxyl-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 106-107°C;

3-[(3,5-difluoro-6-[3-1H-imidazol-1-yl)phenoxy]-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 9.9 (br,4), 8.3 (s,1), 7.8 (s,1), 7.65 (m,6), 7.3 (t,1), 7.15 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-nitrophenoxy)pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.1 (br,4), 8.05 (m,2), 7.7 (m,2), 7.6 (m,2), 7.5 (m,2), 2.45 (s.3) 1.8 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-[3-(methylsulfonyl)amino]phenoxy]pyridin2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10 (br,4), 7.5 (m,3), 7.4 (d,1), 7.15 (t,1), 6.85 (d,1), 6.8 (t,1), 6.66 (dd,1), 2.83 (s,3), 2.36 (s,3) 1.74 (s,3) ppm;

3-[(3,5-difluoro-6-(3-methylcarbonylaminophenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.3 (br,4), 10.1 (s,1), 7.4-7.7 (m,5), 7.25 (m,2), 6.8 (m,1), 2.4 (s,3), 2.1 (s,3), 1.8 (s,3) ppm;

3-[(3,5-difluoro-6-(4-dimethylaminomethylphenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, acetic acid salt; m.p. 103-105°C;

3-[(3,5-difluoro-4-methyl-6-(3-(morpholin-4-yl)phenoxy)pyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 194-196°C;

3-[(3,5-difluoro-4-methyl-6-(3-(1-pyrrolidinoyl)phenoxy)pyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 162-164°C;

3-[(3,5-difluoro-4-methyl-6-(3-(4-morpholinoyl)phenoxy)pyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 123-126°C;

3[(3,5-difluoro-4-methyl-6-(3-dimethylaminocarbonylphenoxy)pyridin-2-yl)oxy]-benzamidine, acetic acid salt; m.p. 198-200°C;

3-[(3,5-difluoro-4-methyl-6-(3-(carboxyl(hydroxy)methylphenoxy)pyridin-2-yl)oxy]-benzamidine, acetic acid salt; NMR (DMSO-d₆) 10 (br,4), 7.4-7.7 (m,6), 7.25 (m,3), 7.15 (m,1), 7.05 (m,1), 4.82 (s,1), 2.4 (s,3). 1.8 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-[3-(1-oxoethyl)]phenoxy]pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.2 (br,4), 7.75 (m,1), 7.65 (m,1), 7.4-7.6 (m,6), 2.5 (s,3), 2.41 (s,3), 1.75 (s,3) ppm;

3-[(3, 5-difluoro-4-methyl-6-[3-(2-methyl-1-oxopropyl)]phenoxy]pyridin-2-yl)oxy]-benzamidine, acetic acid salt; NMR (CDCl₃) 10.2 (br,4), 7.7 (m,1), 7.2-7.6 (m,7), 3.45 (m,1), 2.39 (s,3), 1.88 (s,3), 1.14 (m,6) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(dimethylaminocarbonyl)(hydroxy)methylphenoxy)-pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10 (br,4), 7.55 (m,3), 7.4 (m,1), 7.3 (t,1), 7.1 (m,3), 5.35 (s,1), 2.82 (s,6), 2.40 (s,3), 1.78 (s,3) ppm;

3-[(3,5-difluoro-4-methyl-6-(3-(dimethylaminocarbonyl)(methoxy)methylphenoxy]pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10 (br,4), 7.5 (m,4), 7.4 (m,1), 7.3 (m,2), 7.15 (d,1), 7.05 (m,2), 4.5 (s,1), 3.3 (s,3), 2.4 (s.3), 1.78 (s,3) ppm; and

4-methoxy-3-[(3,5-difluoro-4-(ethoxycarbonylmethyl)(methyl)amino-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine, acetic acid salt.

EXAMPLE 4

3-[(3,5-Difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, Acetic Acid Salt

[0114] 

A. To 3-[(3,5-difluoro-6-[3-dimethylaminophenoxy]-4-methylpyridin-2-yl)-oxy]benzonitrile (1.4 g, 3.7 mmol) dissolved in ethanol (100 mL) and cooled to -10°C was bubbled hydrochloric acid (g) until saturated. The mixture was allowed to warm to ambient temperature and the solvent was removed in vacuo. The residue was dissolved in ethanol (50 mL) and heated at reflux while ammonia (g) was bubbled through the reaction mixture for 2 hours. The solvent was removed in vacuo and the residue was partitioned with 2 N aqueous potassium hydroxide and methylene chloride. The organic layer was separated and dried (MgSO₄). Acetic acid (1 mL) was added and the solvent was removed in vacuo. Crystallization from ether gave 3-[(3,5-difluoro-6-(3-dimethyl-aminophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 176-179°C.

B. In a similar manner, the following compounds were made:

3-[(3,5-difluoro-6-(3-(2-(dimethylamino)ethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 214-216°C;

3-[(3,5-difluoro-6-(3-aminocarbonylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, hydrochloride; NMR (DMSO-d₆) 9.4 (s,2), 9.25 (s,2), 9.1 (s,1), 7.6 (m,2), 7.55 (m,2), 7.4 (s,1), 7.2 (t,1), 7.05 (d,1), 6.6 (d,1). 6.1 (s,2), 2.4 (s,3), 2.1 (s,3), 1.8 (s,3) ppm;

3-[(3,5-difluoro-6-(3-ethoxycarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 198-199°C;

3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy]-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 160-163°C;

3-[(3,5-difluoro-6-[3-(ethylamino)phenoxyl-4-methylpyridin-2-yl)oxy]-benzamidine, acetic acid salt; m.p. 193-196°C;

3-[(6-(3-diethylaminophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 196-197°C;

3-[(3,5-difluoro-4-methyl-6-[3-(phenylamino)phenoxy]pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.0 (br,4), 8.4 (s,1), 7.4-7.7 (m,4), 7.3 (t,2), 7.2 (t,1), 7.1 (d,2), 6.9 (m,2), 6.8 (s,1), 6.5 (d,1), 2.4 (s,3), 1.8 (s,3) ppm;

3-[(3,5-difluoro-6-(3-methylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.3 (br,4), 8.5 (s,1), 7.6 (d,1), 7.55 (m,3), 7.4 (m,3), 2.8 (d,3), 2.4 (s,3), 1.75 (s,3) ppm;

3-[(3,5-difluoro-6-(3-(4-methylpiperazin-1-oyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.3 (br,4), 7.6 (m,3), 7.45 (m,2), 7.25 (m,1), 7.1 (m,2), 3.6 (br,2), 3.2 (br,2), 2.4 (s,3), 2.35 (br,2), 2.2 (br,2), 2.2 (s,3), 1.8 (s,3) ppm;

3[(3,5-difluoro-6-(3-(piperidin-1-oyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.3 (br,4), 7.6 (m,3). 7.45 (m,2), 7.2 (d,1), 7.15 (m,2), 3.6 (br,2), 3.2 (br,2), 2.4 (s,3), 1.8 (s,3) 1.3-1.6 (m,6) ppm;

3-[(3,5-difluoro-6-(3-(methyl)(benzyl)aminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 167-169°C;

3-[(3,5-difluoro-6-(3-(methyl)(2-pyridin-1-ylethyl)aminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 145-150°C;

3-[(3,5-difluoro-6-(3-(methyl)(ethyl)aminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.2 (br,4), 8.5 (m,1), 7.1-7.7 (m,8), 3.4 (br,1), 3.05 (br,1), 1.8 (m,3), 2.4 (s,3), 1.75 (s,3) 1.1 (m,1.5), 1.0 (m,1.5) ppm;

3-[(3,5-difluoro-6-(3-diethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.3 (br,4), 7.5 (m,3). 7.2 (m,2), 7.2 (d,1), 7.1 (m,2), 3.4 (br,2), 3.05 (br,2), 2.4 (s,3), 1.8 (s,3) 1.15 (br,3), 1.0 (br,3) ppm;

3-[(3,5-difluoro-6-(3-(carboxyethyl)aminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, ethyl ester, acetic acid salt;

3-[(6-(3-chlorophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 200-202°C;

3-[(3,5-difluoro-4-methyl-6-(3-trifluoromethylphenoxy)pyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 192-193°C;

3-[(3,5-difluoro-6-(3-methoxyphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 182-185°C;

3-[(3,5-difluoro-6-(3-fluorophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 208-209°C;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-4-methyl benzamidine, acetic acid salt; m.p. 192-193°C;

3-[(3,5-difluoro-4-methyl-6-[3-(phenyl)oxomethyl]phenoxy]pyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 162-165°C;

3-[(3,5-difluoro-6-(3-hydroxyphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 114-117°C;

5-[(3,5-difluoro-6-(3-dimethylaminophenoxyl-4-methylpyridin-2-yl)oxy]-2-methoxybenzamidine, acetic acid salt; NMR (DMSO-d₆) 9.8 (br,4), 7.75 (d,1), 7.7 (s,1), 7.3 (d,1), 7.05 (1,1), 6.45 (d,1), 6.3 (s,1), 6.15 (d,1), 3.8 (s,3), 2.85 (s,6), 2.4 (s,3), 1.8 (s,3) ppm;

3-[(6-(3-ethoxycarbonylmethylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]-benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.0 (br,4), 7.55 (m,3), 7.45 (m,1), 7.25 (m,1), 7.05 (m,3), 4.05 (q,2), 3.65 (s,2), 2.4 (s,3), 1.8 (s,3), 1.2 (t,3) ppm;

3-[(6-(-ethoxycarbonylmethylphenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzamidine;

3-[(6-(3-(2-(ethoxycarbony)ethyl)phenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzenepropionic acid, ethyl ester, acetic acid salt; NMR (DMSO-d₆) 10.2 (br,4), 7.55 (m,3), 7.45 (m,1), 7.25 (t,1), 7.0 (m,3), 4.05 (q,4), 2.8 (t,2), 2.6 (m,2), 2.4 (s,3), 1.8 (s,3), 1.2 (t,3) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-2,6-dimethoxybenzamidine, acetic acid salt; m.p. 109-111°C;

3-[(3,5-difluoro-6-(3-(2-hydroxyethyl)phenoxyl-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; m.p. 179-182°C;

4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 9.6 (br,4), 7.7 (d,1), 7.6 (s,1), 7.3 (t,1), 7.2 (d,1), 7.05 (d,1), 7.0 (d,1), 6.9 (s,1), 3.8 (s,3), 3.1 (s,6), 2.95 (s,3), 2.8 (s,3), 1.75 (s,3) ppm;

4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 10.0 (br,4), 7.65 (m,2), 7.3 (m,1), 7.2 (m,1), 7.0 (m,3), 4.1 (q,2), 3.8 (s,3), 3.7 (m,2), 3.3 (m,2), 3.0 (s,3), 2.8 (s,3), 2.7 (m,1), 2.0 (m,2), 1.75 (s,3), 1.25 (t,3) ppm; and

4-methoxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 9.2 (br,4), 7.8 (d,1), 7.7 (s,1), 7.3 (m,2), 7.0 (m,3), 4.1 (q,21, 3.8 (s,3), 3.7 (m, 1), 3.4 (m,5), 3.0 (s,3), 2.8 (s,3), 2.7 (m,1), 2.0 (s,3), 1.8 (m,4), 1.1 (t,3) ppm.

EXAMPLE 5

4-Amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-benzamidine, Acetic Acid Salt

[0115] 

A. In a manner similar to Example 1 above, 4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzenecarbonitriie was reacted with hydrogen chloride and ammonia. The resulting residue was purified by HPLC on a C18 Dynamax column with a 20-80% acetonitrile in water gradient with 0.1% trifluoroacetic acid and the material was partitioned with ethyl acetate and aqueous sodium bicarbonate. The organic layer was separated, dried (MgSO₄), and the solvent was removed in vacuo. The residue was dissolved in water, acidified with acetic acid, and the solvent removed to give 4-amino-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)-oxy]benzamidine, acetic acid salt; NMR(DMSO-d₆) 10 (br,4), 7.45 (m,2), 7.03 (t,1), 6.79 (d,1), 6.44 (dd,1), 6.33 (t,1), 6.29 (d,1), 6.16 (s,1), 3.36 (s,2). 2.84 (s.6), 2.38 (s,3), 1.76 (s,3) ppm.

B. In a similar manner, the following compound was made:

4-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)amino]-3-hydroxybenzamidine, acetic acid salt; NMR (DMSO-d₆) 10.94 (s,1),9.01 (S,2), 8.71 (S,2), 7.86 (d,1), 7.65 (S,1), 7.26 (t,1), 7.19 (d,1), 6.89 (dd,1), 6.64 (dd,1), 6.54 (m,1), 6.44 (dd,1), 3.4 (s,1), 2.90 (s,6), 2.32 (s,3) ppm.

EXAMPLE 6

4-Hydroxy-3-[(3.5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, Trifluoroacetic Acid Salt

[0116] 

A. To 5-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]-4-methoxybenzamidine, trifluoroacetic acid salt (0.80 g, 1.9 mmol) in methylene chloride (70 mL) at -78°C was added boron tribromide (1 M in methylene chloride, 9 mL, 9 mmol). The reaction was warmed to ambient temperature. After stirring for 16 hours, the reaction was concentrated and purified by HPLC as described above in Example 5 to give 4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.06 (s,2), 8.88 (s,2), 7.67 (m,1), 7.62 (d,1), 7.1 (d,1), 7.04 (t,1), 6.45 (d,1), 6.32 (m,1), 6.23 (d,1), 2.85 (s,6), 2.4 (s,3) ppm.

B. In a similar manner, the following compounds were made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 9.0 (s,2), 8.8 (s,2), 7.6 (m,2), 7.3 (t,1), 7.0 (m,4), 3.1 (s,6), 2.95 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 9.0 (s,2), 0.9 (s.2), 7.55 (m,2), 7.3 (t,1), 7.0 (m,4), 4.1 (q,2), 3.6 (m,2), 3.3 (m,2), 3.0 (s,3), 2.8 (s,3), 2.6 (m,1), 2.0 (m,2), 1.7(s,2), 1.15 (t,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, acetic acid salt; NMR (DMSO-d₆) 9.2 (br,4), 7.6 (m,2), 7.3 (t,1), 7.0 (m,4), 4.1 (q,2), 3.8 (s,3), 3.2-3.7 (m,4), 3.0(s,3), 2.8(s,3), 2.7 (m,1), 2.0 (s,3), 1.8 (m,4), 1.1 (t,3) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 9.1 (s,2), 8.85 (s,2), 7.9 (t,1), 7.6 (m,2), 7.4 (t,1), 7.15 (m,2), 7.05 (m,2), 6.75 (d,1), 6.7 (d,1), 2.95(s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(4-methylpiperazin-1-oyl)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 10.1 (br,1), 9.05 (s,2), 8.85 (s,2), 7.6 (m,2), 7.4 (t,1), 7.2 (m,21, 7.05 (m,21, 6.8 (s,1), 6.7 (s,1), 3.5 (m,8), 2.95 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(5-hydroxy-3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0(s,1),9.9 (s,1), 9.0 (s,2), 8.8 (s,2), 7.6 (m,2), 7.0 (d,1), 6.5 (s,1), 6.4 (s,1), 6.3 (s,1), 2.9 (s,3), 2.7 (s,3), 2.4 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CDCI₃) 11.20 (bs,1), 8.98 (s,2), 8.66 (s,2)_, 7.59 (s,1), 7.53 (d,1), 7.29 (t,1), 7.18-6.92 (m,4), 2.96 (s,3), 2.78 (s,3), 2.36 (s,3), 1.91 (s,1.5) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.1 (s,1), 9.0 (s,2), 8.8 (s,2), 7.6 (m,2), 7.3 (t,1), 7.0-7.1 (m,4), 5.2 (q,2), 3.0 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-hydroxypyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CD₃CN) 8.7 (s,2), 7.5 (s,2), 7.3-7.4 (m,4), 7.2 (dt,1), 7.1 (dd,1), 7.0 (t,1), 6.8 (d,1), 3.1 (s,3), 3.0 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CD₃CN) 9.8 (s,2), 7.3-7.4 (m,4), 7.2 (d,1), 7.1 (d,1), 7.0 (s,1), 6.8 (d,1), 5.1 (t,1), 4.8 (d,4), 3.1 (s,3), 3.0 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-bromo-3-fluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CD₃CN) 10.8 (s,2), 7.3-7.4 (m,4), 7.2 (d,1), 7.1 (d,1), 7.0 (s,1), 6.8 (d,1), 5.1 (m,1), 4.9 (d,1), 4.7 (d,1), 3.8 (d,1), 3.1 (s,3). 3.0 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1,3-dibromoprop-2-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.1 (s,1), 9.0 (s,2), 8.8 (s,2), 7.5-7.6 (m,2), 7.3 (t,1), 7.1 (m,2), 7.0 (m,2), 5.1 (t,1), 3.9 (d,4), 3.0 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((methyl)(carboxymethyl)-mino)pyridin-2-yl)oxy]benzamidine, hydrochloride salt; NMR (DMSO-d₆) 9.0 (s,2), 8.7 (s,2), 7.6 (m,2), 7.2 (1,1), 7.0 (m,4), 4.1 (s,2), 3.2 (s,3), 2.9 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-carboxypyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.12 (s,2), 9.16 (s,2), 9.03 (s,2), 7.3 (m,9), 2.99 (s,3), 2.87 (s,3) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonyl)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 9.06 (s,2), 8.76 (s,2), 8.3 (s,1), 7.85 (s,1), 7.3 (m,9), 2.98 (s,3), 2.86 (s,3) ppm;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(dimethylaminocarbonyl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 10.95 (s,1), 9.08 (s,2), 8.72 (s,2), 7.3 (m,7), 6.72 (s,1), 6.66 (s,1), 2.95 (m,12) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

C. In a similar manner, the following compounds are made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-hydroxy4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-[1-methylimidazol-2-yl)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine.

EXAMPLE 7

4-Hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(piperidin-1-yl)-pyridin-2-yl)oxy]berrzamidine, Trifluoroacetic Acid Salt

[0117] 

A. In a manner similar to Example 1, 3-[(6-(5-cyano-2-(benzyloxy)phenoxy)-3,5-difluoro-4-(piperidin-1-yl)pyridin-2-yl)oxy]-N,N-dimethylbenzamide was reacted with HCI and ammonia. The solvent was removed in vacuo. The material was dissolved in methanol and Pd(C) was added. The reaction was placed under an atmosphere of hydrogen at 3,45·10⁵ Pa for 2 hours. The reaction was filtered through celite® and the solvent was removed in vacuo. The material was partially dissolved in 0.25 N aqueous potassium hydroxide and the solid was removed by filtration. The solid was s purified by HPLC as described above in Example 5 to give 4-hydroxy-3-[(3,5-difluoro-6-(3-dimethyl-aminocarbonylphenoxy)-4-(piperidin-1 yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt, as the final product; NMR (DMSO-d₆) 11.0 (s,1), 9.0 (s,2), 8.7 (s,2), 7.6 (m,2), 7.3 (t,1), 7.0 (m,4), 3.4 (m,4), 2.95 (s,3), 2.8 (s,3), 1.65 (m,6) ppm.

B. In a similar manner, the following compounds were made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.2 (s,1), 10.3 (br,1), 9.0 (s,4), 7.6 (m,2), 7.3 (m,2), 7.0 (m,4), 3.6 (m,8), 3.0 (s,3), 2.9 (s,3), 2.8 (s,3), 1.65 (m,6) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(ethoxycarbonylmethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine, acetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophenoxy)-4-(ethoxycarbonyl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CDCl₃) 11.14 (s,1), 9.37-8.88 (m,8), 7.76-7.06 (m,9), 4.35 (q,2), 1.32 (t,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(morpholin-4-yl)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.0 (s,2), 8.6 (s,2), 7.5 (m,2), 7.3 (t,1), 7.0 (m,4), 3.7 (m,4), 3.4 (m,4), 2.9 (s,3), 2.8 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(methyl)(phenyl)aminocarbonylpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonylphenoxy]pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(prop-2-oxycarbonyl)methylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidinatrifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(ethoxycarbonyl)ethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(ethoxycarbonyl)methylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-guanidinophenoxy)-4-(1-(ethoxycarbonyl)methylpiperidin-4-yl-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(ethoxycarbonylmethy))-piperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.35 (s,1), 10.41 (s,1), 9.03 (d,4), 7.35-7.62 (m,6), 7.0 (d,1), 5.57 (s,1), 4.64 (dd,1), 4.22 (q,2), 4.05 (dd.2), 3.95 (dd,1), 3.78 (d,1), 3.65 (d,1), 2.96 (s,3), 2.75 (m,1), 2.55 (m,1), 1.23 (t,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-methoxycarbonylmethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-aminocarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-2-(3,5-di(ethoxycarbonyl)phenoxy)pyridin-4-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-benzylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbony)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(dimethylaminomethyl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimida2ol)n-2-yl)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophenoxy)-4-(2-metoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-amidinophenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difiuoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chloro-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethyl-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-ethoxycarbonylmethylpiperazinyl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(methyl)(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(tetrahydrofuran-3-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylamindcarbonylphenoxy)-4-(piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(piperidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(carboxymethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-2-methoxypyridin-4-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-2-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-4-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[3-(3-dimethylaminocarbonylphenoxy)-4-(methylamino)carbonylaminophen-1-yloxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3-(3-dimethylaminocarbonylphenoxy)-2,4,6-trichloro-5-fluoro-phen-1-yl)oxy]-benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[(1-(1-(methoxycarbonyl)ethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxyl-4-(2-methoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-(1-(hydroxymethyl)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine,trifluoroaceticacid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-(prop-2-oxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-(2-(methoxy)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-n-butoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-[(2-(2-hydroxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-[(2-(2-methoxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine,trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-(aminocarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(2-(methoxycarbonyl)ethenyl)phenoxylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-(2-chloro-1 -methylethoxycarbonyl)phenoxy) pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

C. In a similar manner, the following compounds are made:

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-methyl-1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(1-methyl-1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(1-methyl-1-(ethoxycarbonyl)ethyl) piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(1-methyl-1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxyl-4-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-aminocarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(5-aminocarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(5-aminocarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(5-aminocarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-methylcarbonylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-methylcarbonylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-methylcarbonylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-methylcarbonylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((ethoxycarbonyl)methoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((ethoxycarbonyl)-methoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((ethoxycarbonyl)-methoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((ethoxycarbonyl)-methoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-ethyl-5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethyl-5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-ethyl-5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-ethyl-5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(tetrazol-5-ylmethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(tetrazol-5-ylmethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(tetrazol-5-ylmethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-(tetrazol-5-ylmethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-12-methoxy-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-diftuoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chloro-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-chloro-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-chloro-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-chloro-4-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chlorophenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-chlorophenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidinolphenoxy)-4-(2-chlorophenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-chlorophenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxyl-4-(1-ethoxycarbonyl-1-methylethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonyl-1-methylethylpiperIdin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-ethoxycarbonyl-1-methylethylpiperidin-4-yloxy)pyridin-2-yl)oxy] benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4-(1-ethoxycarbonyl-1-methylethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((2-ethoxycarbonylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((2-ethoxycarbonylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((2-ethoxycarbonylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((2-ethoxycarbonylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(morpholin-4-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(morpholin-4-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(morpholin-4-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(piperidin-1-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(piperidin-1-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxyl-4-(piperidin-1-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-4-methoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-5-(3-(1-methylimidazol-2-yl)phenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(prop-2-oxycarbonyl)methylpiperidin-4-yloxy)pyridin-2-yl)-oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(prop-2-oxyycarbonyl)methylpiperidin-4-yloxy)pyridin-2-yl)-oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-1-methylimidazol-2-yl)phenoxyl-4-(1-(prop-2-oxycarbonyl)methylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(ethoxycarbonyl)ethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(ethoxycarbonyl)ethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxyl-4-(1-(ethoxycarbonyl)ethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylamipocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-ethoxycarbonylmethylpiperidin-4-yloxy)pyridin-2-yl]oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbony)phenoxy)-4-(4-(1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-5-(3-lguanidino)phenoxy)-4-(4-(1-(ethoxycarbonyl)-ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-ethoxycarbonylmethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl]phenoxy)-4-(4-ethoxycarbonyimethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamide;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-ethoxycarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-dichloro-6-[3-(1-methylimidazolin-2-yl)phenoxy)-4-17 -benzylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-dichloro-6-(3-(guanidino)phenoxy)-4-11-benzylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-dichloro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(-benzylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino(phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4(2.3 dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4 (3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-ethoxycarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-chloro-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-chloro-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-chloro-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethyl-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethyl4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethyl-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine; .

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-12-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((methyl)-(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-4-((methyl)(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methyhmidazol-2-yl)phenoxy)-4-((methyl)-(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy]-4-((piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-(1-(methoxycarbonyl)ethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-(l-(methoxycarbonyl)ethylpiperidin-4-yl)aminolpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-(1-(methoxycarbonyl)ethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-(1-(hydroxymethyl)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-Iguanidino)phenoxyl-4-(2-methoxy-4-(1 -(hydroxymethyl)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-diftuoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-(1-(hydroxymethyl)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-12-methoxy-4-(prop-2-oxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-(prop-2-oxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-(prop-2-oxycarbony))phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-13-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-(2-(methoxy)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-(2-(methoxy)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-(2-(methoxy)ethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-n-butoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-n-butoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-n-butoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-((2-(2-hydroxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-((2-12-hydroxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-((2-(2-hydroxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-((2-(2-methoxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-((2-(2-methoxyethoxy)ethoxy)carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine9;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-((2-(2-methoxyethoxy)ethoxy) carbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-(aminocarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-(aminocarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl(phenoxy(-4-(3-(2-(aminocarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(2-(methoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy4-(2-chloro-1-methylethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-(2-chloro-1-methylethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-(2-chloro-1-methylethoxycarbonyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(2-(ethoxycarbonyl)-ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-(2-tethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy) -4-(4-methylpiperazin-1 -yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-methylpyridin2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-methylpyridin-2-yl) oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine; .

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxyl-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine.

EXAMPLE 8

4-Hydroxy-3-[(3,5-difluoro-6-(3-(imidazol-1-yl)phenoxy)-4-(carboxy)-pyridin-2-yl)oxy]benzamidine, Trifluoroacetic Acid Salt

[0118] 

A. In a manner similar to Example 6, 2-(5-amidino-2-hydroxyphenoxy)-6-(3-(imidazol-1-yl)phenoxy)pyridine-4-carboxylic acid, ethyl ester was reacted with boron tribromide. The resulting oil was dissolved in 6 N HCI and heated at reflux for 2 hours. Concentration of the mixture in vacuo and purification by HPLC as described above in Example 5 gave 4-hydroxy-3-[(3,5-difluoro-6-(3-(imidazol-1-yl)phenoxy)-4-(carboxy)pyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d6, TFA) 9.7 (s,1), 9.0 (s,2), 8.8 (s,2), 8.3 (s,1), 7.9 (s,1), 7.6 (m,5), 7.3 (m,1), 7.1 (m,2), 7.0 (m,1) ppm.

B. In a similar manner, the following compound was made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(carboxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.0 (s,1), 9.1 (s,2), 8.7 (s,2), 7.7 (m,2), 7.2 (m,2), 7.0 (s,1), 6.8 (s,1), 6.6 (d,1), 6.4 (m,2), 2.8 (s,6) ppm.

EXAMPLE 9

3,3'-[4-Aminocarbonyl-2,6-pyridinediylbis(oxy)]bis(benzamidine), Trifluoroacetic Acid Salt

[0119] 

A. In a manner similar to Example 1 above, reaction of 3,3'-[4-ethoxy-carbonyl-2,6-pyridinediylbis(oxy)]bis(benzonitrile) gave 3,3'-[4-aminocarbonyl-2,6-pyridinediylbis(oxy)]-bis(benzamidine), which was purified by HPLC as described above in Example 5 to give the trifluoroacetic acid salt, m.p. >210°C; NMR (DMSO-d₆) 9.3 (s,4), 9.1 (s,4), 8.3 (s,1), 7.8 (s.1), 7.65 (m,4), 7.55 (m,4), 7.2 (s,2) ppm.

B. In a similar manner, the following compounds were made:

3,3'-[3-aminocarbonyl-2,6-pyridinediylbis(oxy)]bis(benzamidine), trifluoroacetic acid salt; NMR (DMSO) 9.45 (br s,4), 9.35 (br s,4), 8.4 (d,1), 7.4-7.9 (m,10), 6.95 (d,1) ppm; and

4-methoxy-3-[(6-(3-dimethylaminophenoxyl-4-aminocarbonylpyridin-2-yl)oxy]benzamidine hydrochloride, NMR (DMSO-d₆) 9.3 (s,2), 9.1 (s,2), 8.3 (s,1), 7.8 (m,2), 7.3 (s,1), 7.1 (m,3), 6.9 (s.1), 6.5 (d,1), 6.3 (m,2), 3.8 (s,3), 2.8 (s,6) ppm.

EXAMPLE 10

2,6-bis(3-Amidinophenoxy)pyridine-3-carboxylic acid, Dihydrochloride

[0120] 

A. In a manner similar to Example 2 above, 2,6-bis(3-amidinophenoxy)-pyridine-3-carboxylic acid, ethyl ester (0.20 g, 0.31 mmol) was dissolved in 5 M HCI and heated for 2 hours at 80 °C. The solvent was removed in vacuo to give 2,6-bis(3-amidinophenoxy)-pyridine-3-carboxylic acid, dihydrochloride; NMR (DMSO-d₆) 9.5 (br s,4), 9.35 (br s,4), 8.45 (d,1), 7.7 (m,2), 7.6 (m,2), 7.5 (m,4), 6.95 (d,1) ppm.

B. In a similar manner, the following compounds were made and purified by HPLC as described above in Example 5:

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimetriylaminophenoxy)-4-(4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(ethoxycarbonylmethoxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-carboxyethyl)-phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methyiimidazolin-2-yl)phenoxy)-4-(3-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(dimethylaminomethyl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chloro-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)aminolpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine,trifluoroaceticacidsalt;NMR (DMSO-d₆) 11.25 (s,1), 10.30 (s,1), 9.03 (br s,4), 7.58-7.55 (m, 2), 7.50 (t,1), 7.38-7.31 (m,3), 7.03 (d,1), 4.10 (s,2), 4.08-3.88 (m,4), 3.66 (m,2), 3.16 (m,2), 2.95 (s,6), 2.26 (m,2), 1.93(m,2) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine, hydrochloride salt; NMR (DMSO-d₆) 11.25 (s,1), 10.45 (s,1), 9.1 (d,4), 7.35 (m,7), 4.18 (s,2), 4.05 (m,4), 3.2 (s,3), 2.95 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

C. In a similar manner, the following compounds are made:

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-methyl-1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(1-methyl-1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(1-methyl-1 -(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1 -methylimidazol-2-yl)phenoxy)-4-(4-(1-methyl-1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(1-(carboxy)ethyl)-piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(1-(carboxy)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4-((2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-(carboxy)ethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-(carboxy)ethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(1-(carboxy)ethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-(1-(carboxy)ethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidirie;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(1-carboxy-1-methylethyl) piperidin-4-yloxy) pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(6-(3-(guanidino)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(carboxymethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(carboxymethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-Cguanidino)phenoxy)-4-(carboxymethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxyl-4-(carboxymethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidinolphenoxyl-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-chloro-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-chloro-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-Cguanidino)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((methyl)-Ccarboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(carboxymethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(carboxymethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxyl-4-(1-(carboxymethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxyl-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine.

EXAMPLE 11

4-Hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-(ethoxycarbonylmethyl)pyrrolidin-3-yloxy)pyridin-2-yloxy]benzamidine, Trifluoroacetic Acid Salt

[0121] 

A. To ethanol (40 mL) was added 4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yloxy]-benzamidine (0.44 g, 0.90 mmol), ethyl bromoacetate (0.15 g, 0.9 mmol), and triethylamine (0.11 g, 1.1 mmol). After stirring for 19 hours, the reaction mixture was concentrated and purified by HPLC as described above in Example 5 to give 4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylamino-phenoxy)-4-(1-(ethoxycarbonylmethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)-oxy]benzamidine, trifluoroacetic acid salt.

B. In a similar manner, the following compounds were made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxy-carbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-Cethoxycarbonylmethyi)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

C. In a similar manner, the following compounds are made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-(ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-(ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-(ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-ethoxycarbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-((1-ethoxycarbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((1-ethoxycarbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine.

EXAMPLE 12

3-[(3,5-Difluoro-6-(3-carboxyphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, Hydrochloride Salt

[0122] 

A. To 3-[(3,5-difluoro-6-(3-ethoxycarbonylphenoxy)-4-methylpyridin-2-yl)-oxy]benzamidine, acetic acid salt (1.0 g, 2.0 mmol) dissolved in methanol (40 mL) was added 5N potassium hydroxide (20 mL). After stirring for 4 hours, the solvent was removed in vacuo. The residue was dissolved in water (50 mL) and acidified with 12 N HCI. The resulting solid was filtered and washed with ether to give 3-[(3,5-difluoro-6-(3-carboxyphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, hydrochloride salt; NMR (DMSO-d₆)9.3 (s,2), 9.1 (s,2), 7.7 (d,1), 7.65 (s,1), 7.3-7.6 (m,6), 2.4 (s,3) ppm. If necessary the material can be further purified by HPLC as described above in Example 5.

B. In a similar manner, the following compounds were made:

3-[(3,5-difluoro-6-(3-(2-carboxyethyl)aminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, m.p. 145-150°C;

3-[(3,5-difluoro-6-(3-(2-carboxyethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.2 (s,2), 7.6 (m,4), 7.25 (t,1), 7.0 (m,2), 6.95 (m,1), 2.8 (t,2), 2.6 (m,2), 2.4 (s,3) ppm;

3-[(3,5-difluoro-6-(3-(carboxymethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 9.3 (s,2), 9.2 (s,2), 7.6 (m,4), 7.25 (t,1), 7.0 (m,3), 3, 4 (s,2), 2.4 (s,3) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxypiperidin1-yl)pyridin-2-yl)oxy]benzamidine; NMR (DMSO-d₆) 9.75 (br,2), 8.5 (br,2), 7.5 (m,2), 7.3 (t,1), 7.0 (m,3), 6.65 (d,1), 3.6 (m,2), 3.2 (m,2), 2.95 (s,3), 2.8 (s,3), 2.3 (m,1), 1.9 (m,2), 1.7 (m,2) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxypiperidin1-yl(pyridin-2-yl)oxy]benzamidine; NMR (DMSO-d₆) 9.75 (br,2). 8.7 (br,2), 7.5 (m,2), 7.3 (t,1), 7.0 (m,3), 6.8 (d,1), 3.2-3.68 (m,4), 2.95 (s,3), 2.8 (s,3), 2.4 (m,1), 2.0 (m,1), 1.8 (m,1), 1.6 (m,2) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.1 (s,1), 9.0 (br,2), 8.9 (br,2), 7.65 (m,2), 7.3 (m,1), 7.0 (m,4), 4.1 (s,2), 3.6 (m,8), 3.0 (s,3), 2.8 (s,3), ppm;

4-hydroxy-3-[(6-(3-amidinophenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (CDCl₃) 11.16 (s,1), 9.38-8.95 (m,8), 7.68-7.04 (m,9) ppm;

3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(N-methyl-N-carboxymethylamino)pyridin-2-yl)oxy]benzamidine; NMR (DMSO-d₆) 9.3 (s,2), 9.2 (s,2), 7.5 (m,4), 7.2 (t,1), 6.7 (m,2), 6.5 (d,1), 4.2 (s,2), 3.2 (s,3), 2.9 (s,6) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.30 (s,1), 10.37 (s,1), 9.00 (s,2), 8.99 (s,2), 7.61 (d,1), 7.57 (dd, 1), 7.52-7.32 (m,4), 7.04 (d,1), 6.55 (s,1), 4.52 (dd,1), 4.02 (dd,2), 3.88 (dd,2), 3.72 (dd,1), 3.58 (d,1), 2.92 (s,3), 2.63 (dd,1), 2.44 (dd,1);

4-hydroxy-3-[(3,5-difluoro-6-3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; NMR (DMSO-d₆) 11.29 (s,1), 10.31 (s,1), 9.05 (s,2). 9.02 (s,2), 7.63-7.57 (m, 2), 7.52 (t,1), 7.42-7.37 (m,3), 7.04 (d,1), 4.92 (br s,1), 4.15 (s,2), 4.09-3.92 (m,4), 3.60-3.40 (m,4), 2.95 (s,3), 2.32-2.10 (m,4) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine; NMR (DMSO-d₆) 11.34 (s,1), 10.46 (s,1), 9.21 (s,2), 8.99(s,2), 7.70 (5,1), 7.63 (d, 1), 7.54 (t,1), 7.43-7.40 (m,2), 7.15 (d,1), 4.96 (br s,1), 4.12-4.09 (m,2), 3.96-3.90 (m,2), 3.40-3.20 (m,4), 2.97 (s,3), 2.40-2.30 (m,2), 2.28-2.14 (m,2), 1.54 (s,6) ppm;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(carboxymethyl)lmethyl)-aminocarbonylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difiuoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypent-1-oxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)(carboxymethyl)aminocarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-carboxymethoxypyridin-2-yl(oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-(carboxymethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(carboxymethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-(2,4-dimethylimidazol-1-yl)phenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-(2-methylimidazol-1-yl)phenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-13-(4-methylimidazol-1-yl)phenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidin, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-(morpholin-4-ylmethyl)phenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(carboxy)pyridin2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(carboxy)pyridin2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-amino-3-[(3,5-difluoro-6-(3.dimethylaminophenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

3-hydroxy-4-[(6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

3-hydroxy-4-[(6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(carboxy)pyridin-2-yl)oxy]benzamidine, trifiuoroacetic acid salt;

4-hydroxy-3-[(6-(3-dimethylaminocarbonylphenoxy)-4-(carboxymethyl)-(methyl)aminocarbonylpyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(6-(3-dimethylaminophenoxyl-4-(4-carboxymethylpiperazin-1-oyl)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

C. In a similar manner, the following compounds are made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-chloro-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-(2-carboxyethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl(phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-carboxypiperidin-1-y1lpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(5-carboxypent-1-oxy)pyridin)-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(5-carboxypent-1-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(5-carboxypent-1-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-aminocarbonyl5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidinolphenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difiuoro-6-(3-(guanidino)phenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxyl-4-(5-carboxypyrrotidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

EXAMPLE 13 (Reference Example)

3-[(3,5-Difluoro-6-(3-((phenyl)hydroxymethyl)phenoxy)-4-methylpyridin-2-yl)oxy]benzamidine. Trifluoroacetic Acid Salt

[0123] 

A. To 3-[(3,5-difluoro-4-methyl-6-(3-((phenyl)oxomethyl)phenoxy)-pyridin-2-yl)oxy]benzamidine. acetic acid salt, (0.10 g, 0.19 mmol) in methanol was added Pd-C (75 mg). After stirring under hydrogen for 2.5 hours, the reaction was filtered, concentrated in vacua, and purified by HPLC as described above in Example 5 to give 3-[(3,5-difluoro-6-(3-((phenyl)hydroxymethyl)phenoxy)-4-methyl-pyridin-2-yl)oxy]benzamidine,trifluoroaceticacidsalt; NMR (DMSO-d₆) 9.45 (s,2), 9.35 (s,2), 7.55 (m,4), 7.1-7.4 (m,8), 6.95 (m,1), 5.64 (s,1). 2.4 (s,3) ppm.

EXAMPLE 14

4-Hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, Trifluoroacetic Acid Salt

[0124] 

A. To ethanol (8 mL) was added 4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonylphenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine (0.16 g, 0.20 mmol), ethylacetimidate hydrochloride (74 mg, 0.6 mmol), and triethylamine (0.10 g, 1.0 mmol). After stirring for 2 hours, the reaction mixture was concentrated and purified by HPLC as described above in Example 5 to give 4-hydroxy-3-[(3,5-dichloro-6-(3-dimethylaminocarbonyl-phenoxy)-4-(1-(1-iminoethyl) pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

B. In a similar manner, the following compounds were made:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]banzamidine, trifluoroacetic acid salt 6922.

C. In a similar manner, the following compounds are made:

4-hydroxy-3,[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-(1-iminoethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-(1-(1-iminoethyl)-pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine, trifluoroacetic acid salt.

EXAMPLE 15

[0125] This example illustrates the preparation of representative pharmaceutical compositions for oral administration containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g., 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimida2olin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine:

A.	Ingredients	% wt./wt.
	Compound of the invention	20.0%
	Lactose	79.5%
	Magnesium stearate	0.5%

[0126] The above ingredients are mixed and dispensed into hard-shell gelatin capsules containing 100 mg each.

B.	Ingredients	% wt./wt.
	Compound of the invention	20.0%
	Magnesium stearate	0.9%
	Starch	8.6%
	Lactose	79.6%
	PVP (polyvinylpyrrolidine)	0.9%

[0127] The above ingredients with the exception of the magnesium stearate are combined and granulated using water as a granulating liquid. The formulation is then dried, mixed with the magnesium stearate and formed into tablets with an appropriate tableting machine.

C.	Ingredients
	Compound of the invention	0.1 g
	Propylene glycol	20.0 g
	Polyethylene glycol 400	20.0 g
	Polysorbate 80	1.0 g
	Water	q.s. 100 mL

[0128] The compound of the invention is dissolved in propylene glycol, polyethylene glycol 400 and polysorbate 80. A sufficient quantity of water is then added with stirring to provide 100 mL of the solution which is filtered and bottled.

D.	Ingredients	% wt./wt.
	Compound of the invention	20.0%
	Peanut Oil	78.0%
	Span 60	2.0%

[0129] The above ingredients are melted, mixed and filled into soft elastic capsules.

E.	Ingredients	% wt./wt.
	Compound of the invention	1.0%
	Methyl or carboxymethyl cellulose	2.0%
	0.9% saline	q.s. 100 mL

[0130] The compound of the invention is dissolved in the cellulose/saline solution, filtered and bottled for use.

EXAMPLE 16

[0131] This example illustrates the preparation of a representative pharmaceutical formulation for parenteral administration containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g., 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]-benzamidine:

Ingredients
Compound of the invention	0.02 g
Propylene glycol	20.0 g
Polyethylene glycol 400	20.0 g
Polysorbate 80	1.0 g
0.9% Saline solution	q.s. 100 mL

[0132] The compound of the invention is dissolved in propylene glycol, polyethylene glycol 400 and polysorbate 80. A sufficient quantity of 0.9% saline solution is then added with stirring to provide 100 mL of the I.V. solution which is filtered through a 0.2 µ membrane filter and packaged under sterile conditions.

EXAMPLE 17

[0133] This example illustrates the preparation of a representative pharmaceutical composition in suppository form containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g., 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methyl-imidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylmethy)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine:

Ingredients	% wt./wt.
Compound of the invention	1.0%
Polyethylene glycol 1000	74.5%
Polyethylene glycol 4000	24.5%

[0134] The ingredients are melted together and mixed on a steam bath, and poured into molds containing 2.5 g total weight.

EXAMPLE 18

[0135] This example illustrates the preparation of a representative pharmaceutical formulation for insulation containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g. , 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-carboxyphenoxylpyridin-2-yl)oxy]benzamidine:

Ingredients	% wt./wt.
Micronized compound of the invention	1.0%
Micronized lactose	99.0%

[0136] The ingredients are milled, mixed, and packaged in an insufflator equipped with a dosing pump.

EXAMPLE 19

[0137] This example illustrates the preparation of a representative pharmaceutical formulation in nebulized form containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g., 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)-oxy]benzamidine:

Ingredients	% wt./wt.
Compound of the invention	0.005%
Water	89.995%
Ethanol	10.000%

[0138] The compound of the invention is dissolved in ethanol and blended with water. The formulation is then packaged in a nebulizer equipped with a dosing pump.

EXAMPLE 20

[0139] This example illustrates the preparation of a representative pharmaceutical formulation in aerosol form containing a compound of the invention, or a pharmaceutically acceptable salt thereof, e.g., 4-hydroxy-3-[(3,5-difluoro-6-[(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine:

Ingredients	% wt./wt.
Compound of the invention	0.10%
Propellant 11/12	98.90%
Oleic acid	1.00%

[0140] The compound of the invention is dispersed in oleic acid and the propellants. The resulting mixture is then poured into an aerosol container fitted with a metering valve.

EXAMPLE 21

(In vitro assay for Factor Xa, Thrombin and Tissue Plasminogen Activator)

[0141] This assay demonstrates the activity of the compounds of the invention towards factor Xa, thrombin and tissue plasminogen activator. The activities were determined as an initial rate of cleavage of the peptide p-nitroanilide by the enzyme. The cleavage product, p-nitroaniline, absorbs at 405 nm with a molar extinction coefficient of 9920 M^-1cm^-1.

Reagents and Solutions:

[0142] 

Dimethyl sulfoxide (DMSO) (Baker analyzed grade).

Assay buffer:
   50 mM TrisHCl, 150 mM NaCI, 2.5 mM CaCl₂, and 0.1% polyethylene glycol 6000, pH 7.5.

Enzymes (Enzyme Research Lab.):

1. Human factor Xa stock solution: 0.281 mg/mL in assay buffer, stored at -80°C (working solution (2X): 106 ng/mL or 2 nM in assay buffer, prepare prior to use).

2. Human thrombin stock solution: Stored at -80°C (working solution (2X): 1200 ng/mL or 40 nM in assay buffer, prepare prior to use).

3. Human tissue plasminogen activator (tPA) (Two chains, Sigma) stock solution: 1 mg/mL, stored at -80°C (working solution (2X): 1361 ng/mL in assay buffer, prepare prior to use).

Chromogenic substrates (Pharmacia Hepar Inc.):

1. S2222 (FXa assay) stock solution: 6 mM in dH₂O, store at 4°C (working solution (4X): 656 µM in assay buffer).

2. S2302 (Thrombin assay) stock solution: 10 mM in dH₂O, stored at 4°C (working solution (4X): 1200 µM in assay buffer).

3. S2288 (tPA assay) stock solution: 10 mM in dH₂O, stored at 4°C (working solution (4X): 1484 µM in assay buffer).
   (All substrate working solutions were prepared on assay day 5.)

Standard inhibitor compound stock solution:
   5 mM in DMSO, stored at -20°C.

Test compounds (compounds of the invention) stock solutions:
   10 mM in DMSO, stored at -20°C.

Assay procedure:
   Assays were performed in 96-well microtiter plates in a total volume of 200 µl. Assay components were in final concentration of 50 mM TrisHCl, 150 mM NaCl, 2.5 mM CaCl₂, 0.1% polyethylene glycol 6000, pH 7.5, in the absence or presence of the standard inhibitor or the test compounds and enzyme and substrate at following concentrations: (1) 1 nM factor Xa and 164 µM S2222; (2) 20 nM thrombin and 300 µM S2302; and (3) 10 nM tPA and 371 µM S2288. Concentrations of the standard inhibitor compound in the assay were from 5 µM to 0.021 µM in 1 to 3 dilution. Concentration of the test compounds in the assay typically were from 10 µM to 0.041 µM in 1 to 3 dilution. For potent test compounds, the concentrations used in the factor Xa assay were further diluted 100 fold (100 nM to 0.41 nM) or 1000 fold (10 nM to 0.041 nM). All substrate concentrations used are equal to their K_m values under the present assay conditions. Assays were performed at ambient temperature.

[0143] The first step in the assay was the preparation of 10 mM test compound stock solutions in DMSO (for potent test compounds, 10 mM stock solutions were further diluted to 0.1 or 0.01 mM for the factor Xa assay), followed by the preparation of test compound working solutions (4X) by a serial dilutions of 10 mM stock solutions with Biomek 1000 (or Multiprobe 204) in 96 deep well plates as follows:

(a) Prepare a 40 µM working solution by diluting the 10 mM stock 1 to 250 in assay buffer in 2 steps: 1 to 100, and 1 to 2.5.

(b) Make another five serial dilutions 11:3) of the 4OµM solution (600 µl for each concentration). A total of six diluted test compound solutions were used in the assay.

Standard inhibitor compound (5 mM stock) or DMSO (control) went through the same dilution steps as those described above for test compounds.

[0144] The next step in the assay was to dispense 50 µl of the test compound working solutions (4X) (from 40 uM to 0.164 uM) in duplicate to microtiter plates with Biomek or MP204. To this was added 100 µl of enzyme working solution (2X) with Biomek or MP204. The resulting solutions were incubated at ambient temperature for 10 minutes.

[0145] To the solutions was added 50 p1 of substrate working solution (4X) with Biomek or MP204.

[0146] The enzyme kinetics were measured at 405 nm at 10 seconds intervals for five minutes in a THERMOmax plate reader at ambient temperature.

Calculation of K_i of the test compounds:

[0147] Enzyme rates were calculated as mOD/min based on the first two minutes readings. The IC₅₀ values were determined by fitting the data to the log-logit equation (linear) or the Morrison equation (non-linear) with an EXCEL spread-sheet. Ki values were then obtained by dividing the IC₅₀ by 2. Routinely, Ki(factor Xa) values less than 3 nM were calculated from the Morrison equation.

[0148] Compounds of the invention, when tested in this assay, demonstrated the selective ability to inhibit human factor Xa and human thrombin.

EXAMPLE 22

(In vitro assay for Human Prothrombinase)

[0149] This assay demonstrates the ability of the compounds of the invention to inhibit prothrombinase. Prothrombinase (PTase) catalyzes the activation of prothrombin to yield fragment 1.2 plus thrombin with meizothrombin as the intermediate. This assay is an end point assay. Activity of the prothrombinase is measured by activity of thrombin tone of the reaction products) or by the amount of thrombin formed/time based on a thrombin standard curve (nM vs mOD/min). For determination of IC_5o (PTase) of the compounds of the invention, PTase activity was expressed by thrombin activity (mOD/min).

Materials:

[0150] 

Enzymes:

1. Human factor Va (Haematologic Technologies Inc., Cat# HCVA-0110) working solution: 1.0 mg/mL in 50% glycerol, 2 mM CaCl₂, stored at -20°C.

2. Human factor Xa (Enzyme Res. Lab. cat# HFXa1011) working solution: 0.281 mg/mL in assay buffer (without BSA), stored at -80°C.

3. Human prothrombin (FII) (Enzyme Res. Lab., Cat# HP1002) working solution:
   Diluted FII to 4.85 mg/mL in assay buffer (without BSA), stored at -80°C.

Phospholipid (PCPS) vesicles:

PCPS vesicles (80%PC, 20%PS) were prepared by modification of the method reported by Barenholz et al., Biochemistry (1977), Vol. 16, pp. 2806-2810.

Phosphatidyl serine (Avanti Polar Lipids, Inc., Cat#840032):
   10 mg/mL in chloroform, purified from brain, stored -20°C under nitrogen or argon.

Phosphatidyl Choline (Avanti Polar Lipids, Inc., Cat# 850457):
   50 mg/ml in chloroform, synthetic 16:0-18:1 Palmitoyl-Oleoyl, stored at -20°C under nitrogen or argon.

Spectrozyme-TH (American Diagnostica Inc., Cat# 238L, 50 µmoles, stored at room temperature) working solution: Dissolved 50 µmoles in 10 mL dH₂O.

BSA (Sigma Chem Co., Cat# A-7888, FractionV, RIA grade).

Assay buffer: 50 mM TrisHCl, pH 7.5, 150 mM NaCI, 2.5 mM CaCl₂, 0.1% PEG 6000 (BDH), 0.05% BSA (Sigma, Fr.V, RIA grade).

For one plate assay, prepare the following working solutions:

1. Prothrombinase complex:

(a) 100 µM PCPS (27.5 µl of PCPS stock (4.36 mM) diluted to final 1200 µl with assay buffer.

(b) 25 nM Human factor Va: 5.08 µl of Va stock(1 mg/mL) was diluted to final 1200//1 with assay buffer.

(c) 5 pM Human factor Xa: Dilute Xa stock (0.281 mg/mL) 1:1,220,000 with assay buffer. Prepare at least 1200 p\,

Combine equal volumes (1100 girl) of each component in the order of PCPS, Va and Xa. Let stand at ambient temperature for 5 to 10 minutes and use immediately or store in ice (bring to ambient temperature before use).

2. 6µM Human prothrombin (FII): dilute 124 µL of Fll stock (4.85 mg/mL) to final 1400 µL with assay buffer.

3. 20 mM EDTA/Assay buffer: 0.8 mL of 0.5 M EDTA (pH 8.5) plus 19.2 mL assay buffer.

4. 0.2 mM Spectrozyme-TH/EDTA buffer: 0.44 mL of SPTH stock (5 mM) plus 10.56 mL of 20 mM EDTA/assay buffer.

5. Test compounds (compounds of the invention):

Prepare a working solution (5X) from 10 mM stock (DMSO) and make a series of 1:3 dilution.

Compounds were assayed at 6 concentrations in duplicate.

Assay conditions and procedure:
Prothrombinase reaction was performed in final 50 pL of mixture containing PTase (20 uM PCPS, 5 nM hFVa, and 1 pM hFXa), 1.2 uM human factor II and varied concentration of the test compounds (5 pN\ to 0.021 µM or lower concentration range). Reaction was started by addition of PTase and incubated for 6 minutes at room temperature. Reaction was stopped by addition of EDTA/buffer to final 10 mM. Activity of thrombin (product) was then measured in the presence of 0.1 mM of Spectrozyme-TH as substrate at 405 nm for 5 minutes (10 seconds intervals) at ambient temperature in a THEROmax microplate reader. Reactions were performed in 96-well microtiter plates.
In the first step of the assay, 10 µl of diluted test compound (5X) or buffer was added to the plates in duplicate. Then 10 µl of prothombin (hFII) (5X) was added to each well. Next 30 µl PTase was added to each well, mix for about 30 seconds. The plates were then incubated at ambient temperature for 6 minutes.
In the next step, 50 µl of 20 mM EDTA (in assay buffer) was added to each well to stop the reaction. The resulting solutions were then mixed for about 10 seconds. Then 100 µl of 0.2 mM spectrozyme was added to each well. The thrombin reaction rate was then measured at 405 nm for 5 minutes at 10 seconds intervals in a Molecular Devices microplate reader.

Calculations:
Thrombin reaction rate was expressed as mOD/min. using OD readings from the five minute reaction. IC₅₀ values were calculated with the log-logit curve fit program.
The compounds of the invention demonstrated the ability to inhibit pro-thrombinase when tested in this assay.

EXAMPLE 23

(In vivo assay)

[0151] The following assay demonstrates the ability of the compounds to act as anti-coagulants.

[0152] Male rats (250-330 g) were anesthetized with sodium pentobarbital (90 mg/kg, i.p.) and prepared for surgery. The left carotid artery was cannulated for the measurement of blood pressure as well as for taking blood samples to monitor clotting variables (prothrombin time (PT) and activated partial thromboplastin time (aPTT)). The tail vein was cannulated for the purpose of administering the test compounds (i.e., the compounds of the invention and standards) and the thromboplastin infusion. The abdomen was opened via a mid-line incision and the abdominal vena cava was isolated for 2-3 cm distal to the renal vein. All venous branches in this 2-3 cm segment of the abdominal vena cava were ligated. Following all surgery, the animals were allowed to stabilize prior to beginning the experiment. Test compounds were administered as an intravenous bolus (t =0). Three minutes later (t=3), a 5-minute infusion of thromboplastin was begun. Two minutes into the infusion (t=5), the abdominal vena cava was ligated at both the proximal and distal ends. The vessel was left in place for 60 minutes, after which it was excised from the animal, slit open, the clot (if any) carefully removed, and weighed. Statistical analysis on the results was perfomed using a Wilcoxin-matched-pairs signed rank test.

[0153] The compounds of the invention, when tested in this assay, demonstrated the ability to inhibit the clotting of the blood.

Claims

1. A compound selected from the group consisting of the following formulae:







   wherein

A   is -N=;

Z'   and Z² are independently -O-, -N(R⁸)-, -S-, or -OCH₂-;

R¹   and R³ are independently hydrogen, halo, alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹ -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹², or -N(R⁸)C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹;

R² is   hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -C(O) N(R⁸)R⁹; -N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3); -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²   is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, aminocarbonylalkyl, Calkylaminolcarbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²   is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, and tetrazolylalkyl);

or R²   is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonylalkyl and aralklyl);

or R²   is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴ and R⁷   are independently hydrogen; halo, alkyl, nitro, -OR⁸, -C(O)OR⁸, -C(O)NC(R⁸)R⁹, -N(R⁸)R⁹, -N(H)C(O)R⁸, or -N(H)S(O)₂R¹²;

R⁵ is   -C(NH)NH₂, -C(NH)N(H)OR⁸, -C(NH)N(H)C(O)OR¹², -C(NH)N(H)S(O)₂R¹², -C(NH)N(H)C(O)N(R⁸)R⁹, or -C(NH)N(H)C(O)R⁸;

R⁶   is halo, alkyl, haloalkyl, haloalkoxy, nitro, amino, ureido, guanidino, -OR⁹, -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH₂)_mC(O)N(R⁸)R⁹ (where m is 0 to 3), -CH(OH)C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), -(CH₂)_mC(O)OR⁸ (where m is 0 to 3), -N(H)C(O)R⁸, (1,2)-tetrahydropyrimidinyl (optionally substituted by alkyl), (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazoliny) (optionally substituted by alkyl);

each R⁸ and R⁹   are independently hydrogen, alkyl, aryl, or aralkyl;

R¹⁰   is hydrogen, alkyl, aryl, aralkyl, 1-pyrrolidinyl, 4-morpolinyl, 4-piperazinyl, 4-(N-methyl)piperazinyl, or piperidin-1-yl;

R¹¹   is hydrogen, alkyl or halo; and

R¹²   is alkyl, aryl or aralkyl;

or a pharmaceutically acceptable salt thereof. with the proviso that when the compound is selected from formula IV, and R⁵ and R⁶ are both -C(NH)NH₂, simultaneously
   both of Z¹ and Z² are not -O- or -N(R⁸)-, where R⁸ is H; and
   R² is not H; -N(R⁸)R⁹ where R⁸ and R⁹ are H, -CH₃, or -CH₂CH₃; or -OR⁸ where R⁸ is -CH₃; and wherein the term "alkyl" refers to C₁-C₆ alkyl.

2. The compound selected from formula (It:

   wherein

A   is -N=;

Z¹ and Z²   are independently -O-, -N(R⁶)- or -OCH₂-;

R¹ and R³   are independently hydrogen, fluoro, chloro. haloalkyl. -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, or -N(R⁸)S(O)₂R¹²;

R²   is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -C(O)N(R⁸)R⁹; -N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3); -NCR⁸(CH₂)_n(O)R⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)O(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3l: morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²   is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl. aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl. (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkeny), aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylaminolcarbonylalkenyl, (aralkylamino)carbonylalkenyl/(hydroxyalkoxylcarbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxylalkoxycarbonyl. (lalkoxylalkoxylalkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl)):

or R²   is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, or BikoxycerbonylalkyI);

or R²   is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, or tatrazolylalkyll;

or R²   is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyi, alkoxycarbonyl, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonylalkyi or aralklyl);

or R²   is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1.iminoethyl, cerboxy, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonyl or alkoxycarbonylalkyl);

R⁴   is hydrogen, -OR⁸ or N(R⁸)R⁹;

R⁵   is -C(NH)NH,;

R⁶   is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸R⁹ (where m is 0 to 3), 1-piperidinoyl, 1-pyrrolidinoyl, (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl);

R⁷   is hydrogen, halo, alkyl, -OR⁸, -C(O)N(R⁸)R⁹;

R⁸ and R⁹   are independently hydrogen, methyl, ethyl or phenyl; and

R¹²   is methyl, ethyl, phenyl or benzyl.

3. The compound of Claim 2 wherein

Z¹ and Z²   are independently -O- or -NCH₃-;

R¹ and R³   are independently hydrogen, fluoro, chloro, trifluoromethyl, amino, C(O)N(R⁸)R⁹, or -NHC(O)NHR⁹;

R²   is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁹; -N(R⁸)R⁹; -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²   is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or R²   is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxyalkyl, and alkoxycarbonylalkyl);

or R²   is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy and alkoxycarbonyl);

or R²   is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl and alkoxycarbonylalkyl);

or R²   is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl, alkoxycarbonylalkyi and aralklyl);

or R²   is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴   is hydrogen, amino, hydroxy, or methoxy;

R⁵   is -C(NH)NH₂;

R⁶   is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 1), (1,2)-imidazolyl substituted by alkyl, or 2-imidazolinyl substituted by alkyl;

R⁷   is hydrogen, methoxy, or hydroxy; and

R⁸ and R⁹   are independently hydrogen, methyl, ethyl, or phenyl.

4. The compound of Claim 3 wherein

Z¹ and Z²   are both -O-;

R¹ and R³   are independently hydrogen, fluoro, or chloro;

R⁴   is amino, hydrogen, hydroxy or methoxy;

R⁶   is guanidino, -C(NH)NH₂, -CCO)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 or 1), (1,2)-imidazolyl substituted by methyl, or 2-imidazolinyl optionally substituted by methyl; and

R⁷   is hydrogen or hydroxy.

5. The compound of Claim 4 wherein

R⁴   is hydroxy;

R⁶   is dimethylamino or dimethylaminocarbonyl; and

R⁷   is hydrogen.

6. The compound of Claim 5 selected from the group consisting of the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-propoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbony)phenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-dimethylaminopyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-bromo-3-fluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonyiphenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-methoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(piperidin-1-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(4-methylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(morpholin-4-yl)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxymethylpiperazinyl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonylmethylpiperazinyl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-(morpholin-4-ylmethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl(oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethyiaminophenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-carboxymethoxypyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl]oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl]oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-4-((1-carboxymethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminophenoxy)-4-((methyl)-((carboxymethyl)aminocarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine.

7. The compound of Claim 4 wherein

R⁴   is hydroxy;

R⁶   is (1,2)-imidazolyl substituted by methyl or 2-imidazolinyl substituted by methyl; and

R⁷   is hydrogen.

8. The compound of Claim 7 selected from the group consisting of the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)-(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-(methoxycarbonyl)ethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-(ethoxycarbonyl)ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[3-ethoxycarbonyiphenoxy)pyridin-2-yl)oxy]benzamidine; .

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-[2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazo)in-2-y))phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-4-(3-(1-methylimidazolin-2-yl)phenoxy)-6-(3,5-dicarboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)(phenoxy)-4-(2-chloro-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-1-methylimidazolin-2yl)phenoxy)-4-((1-ethoxycarbonylmethyl)piperidin-4-yl)oxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1 -methylimidazolin-2-yl)phenoxy)-4-(4-(ethoxycarbonylmethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((piperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl(oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylinnidazolin-2-yl)phenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypent-1-oxy)pyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine.

9. The compound of Claim 4 wherein

R⁴   is hydroxy;

R⁶   is guanidino; and

R⁷   is hydrogen.

10. The compound of Claim 9 selected from the group consisting of the follow

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-ethoxycarbonylmethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidine;

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(methyl)(phenyl)aminocarbonylpyridin-2-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidine.

11. The compound of Claim 1 which is selected from formula (VIII:

   wherein

Z¹ and Z²   are independently -O-, -N(R⁸)- or -OCH₂-;

R¹ and R³   are independently hydrogen, fluoro, chloro, haloalkyl, -NCR⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, or -N(R⁸)S(O)₂R¹²;

R²   is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -C(O)N(R⁸)R⁹; -N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (where m is 0 to 3); -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p - is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or R²   is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -C(O)N(R⁸)R⁹, halo, alkyl, carboxy, alkoxycarbonyl, haloalkoxy, haloalkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, aminocarbonylalkyl, (alkylamino)carbonylalkyl, (dialkylamino)carbonylalkyl, (arylamino)carbonylalkyl, (aralkylamino)carbonylalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, ; aminocarbonylalkenyl, (alkylamino)carbonylalkenyl, (dialkylamino)carbonylalkenyl, (arylamino)carbonylalkenyl, (aralkylamino)carbonylalkenyl, (hydroxyalkoxy)carbonyl, (alkoxy)alkoxycarbonyl, (hydroxyalkoxy)alkoxycarbonyl, ((alkoxy)alkoxy)alkoxycarbonyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or   R² is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is 1-piperazinoyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, and alkoxycarbonylalkyl);

or R²   is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy, -C(O)N(R⁸)R⁹, carboxyalkyl, alkoxycarbonyl, or alkoxycarbonylalkyl);

or R²   is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkylcarbonyl, carboxy, -C(O)N(R⁸)R⁹, alkoxycarbonyl, carboxyalkyl, alkoxycarbonylalkyl, or tetrazolylalkyl);

or R²   is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxycarbonyl, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonylalkyl or aralklyl);

or R²   is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of alkyl, aralkyl, amidino, 1-iminoethyl, carboxy, carboxyalkyl, -C(O)N(R⁸)R⁹, alkoxycarbonyl or alkoxycarbonylalkyl);

R⁴   is hydrogen, -OR⁸ or -N(R⁸)R⁹;

R⁵   is -C(NH)NH₂;

R⁶   is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 3), 1-piperidinoyl, 1-pyrrolidinoyl, (1,2)-imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl);

R⁷   is hydrogen, halo, alkyl, -OR⁸, -C(O)N(R⁸)R⁹;

R⁸ and R⁹   are independently hydrogen, methyl, ethyl or phenyl; and

R¹²   is methyl, ethyl, phenyl or benzyl.

12. The compound of Claim 11 wherein

Z¹ and Z²   are independently -O- or -NCH₃-;

R¹ and R³   are independently hydrogen, fluoro, chloro, trifluoromethyl, amino, -C(O)N(R⁸)R⁹, or -NHC(O)NHR⁹;

R²   is hydrogen; halo; alkyl; haloalkoxy; -OR⁸; -C(O)OR⁸; -N(R⁸)R⁹; -N(R⁸)(CH₂)_nC(O)OR⁸ (where n is 1 to 3); N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (where each n is 1 to 3); -O(CH₂)_nC(O)N(R⁸)R⁹ (where n is 1 to 3); -O(CH₂)_pC(O)OR⁸ (where p is 1 to 6); -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (where each n is independently 1 to 3); morpholin-4-yl; 3-tetrahydrofuranoxy;

or   R² is aryloxy (optionally substituted by one or more substituents independently selected from the group consisting of -OR⁸, -CCO)N(R⁸)R⁹ halo, alkyl, carboxy, alkoxycarbonyl, alkoxycarbonylalkyl, carboxyalkyl, alkoxycarbonylalkenyl, carboxyalkenyl, tetrazolyl, morpholin-4-ylalkyl, and (1,2)-imidazolinyl (optionally substituted by alkyl));

or   R² is piperazin-1-yl (optionally substituted by one or more substituents independently selected from the group consisting of alkyl, carboxyalkyl, and alkoxycarbonylalkyl);

or   R² is piperidin-1-yl (optionally substituted by one or more substituents selected from the group consisting of carboxy and alkoxycarbonyl);

or   R² is (3,4)-piperidinyloxy (optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl and alkoxycarbonylalkyi);

or   R² is piperidin-4-ylamino (wherein the amino is optionally substituted by alkyl and the piperidinyl group is optionally substituted by one or more substituents selected from the group consisting of carboxyalkyl, alkoxycarbonylalkyl and aralklyl);

or   R² is 3-pyrrolidinyloxy (optionally substituted by one or more substituents selected from the group consisting of 1-iminoethyl, carboxy, carboxyalkyl, alkoxycarbonyl and alkoxycarbonylalkyl);

R⁴   is hydrogen, amino, hydroxy, or methoxy;

R⁵   is -C(NH)NH₂;

R⁶   is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 to 1), (1,2)-imidazolyl substituted by alkyl, or 2-imidazolinyl substituted by alkyl;

R⁷   is hydrogen, methoxy, or hydroxy; and

R⁸   and R⁹ are independently hydrogen, methyl, ethyl, or phenyl.

13. The compound of Claim 12 wherein

Z¹ and Z²   are both -O-;

R¹ and R³   are independently hydrogen, fluoro, or chloro;

R⁴   is hydrogen, amino, hydroxy or methoxy;

R⁶   is guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (where m is 0 or 1), (1,2)-imidazolyl substituted by methyl, or 2-imidazolinyl optionally substituted by methyl; and

R⁷   is hydrogen or hydroxy.

14. The compound of Claim 13 wherein

R⁴   is hydroxy;

R⁶   is dimethylamino or dimethylaminocarbonyl; and

R⁷   is hydrogen.

15. The compound of Claim 14 selected from the group consisting of the following:

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-2-methoxypyridin-4-yl)oxy]benzamidine; and

4-hydroxy-3-[(3,5-difluoro-6-(3-dimethylaminocarbonylphenoxy)-2-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-4-yl)oxy]benzamidine.

16. A pharmaceutical composition useful in treating a human having a disease-state characterized by thrombotic activity, which composition comprises a therapeutically effective amount of a compound according to any of the preceding claims.

17. Use of a therapeutically effective amount of a compound according to claims 1 - 15 for the manufacture of a medicament for treating a disease-state characterized by thrombotic activity.

18. A compound according to any one of claims 1 - 15 for use as a medicament.

19. The use of claim 17, wherein the medicament is an anti-coagulant.

20. The use of claims 17 or 19, where the treatment involves prophylaxis for long term risk following myocardial infarction, prophylaxis of deep vein thrombosis (DVT) following orthopedic surgery, prophylaxis of selected patients following a transient ischemic attack; treatment of deep vein thrombosis (DVT); treatment associated with surgical intervention such as coronary artery bypass graft and percutaneous transluminal coronary angioplasty; treatment of thrombotic complications associated with acute promyelocytic leukemia, diabetes, multiple myelomas, disseminated intravascular coagulation associated with septic shock, purpura fulminanas associated infection, adult respiratory distress syndrome, unstable angina, and thrombotic complications associated with aortic valve or vascular prosthesis; prophylaxis for thrombotic diseases, in particular in patients who have a high risk of developing such disease.

Ansprüche

1. Verbindung aus der Gruppe bestehend aus den Formeln:







worin

A für -N= steht;

Z¹ und Z² unabhängig voneinander für -O-, -N(R⁸)-, -S- oder -OCH₂- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Halogen, Alkyl, Halogenalkyl, Alkoxy, Halogenalkoxy, Nitro, -N (R⁸) R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹² oder -N(R⁸)C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹ stehen;

R² für Wasserstoff, Halogen, Alkyl, Halogenalkoxy, -OR⁸, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (worin m 0 bis 3 bedeutet), -N(R⁸)(CH₂)_nC(O)OR⁸ (worin n 1 bis 3 bedeutet), -N((CH₂)_nN(R⁸)R⁹) (CH₂)_nC(O)OR⁸ (worin n jeweils 1 bis 3 bedeutet), -O(CH₂)_nC(O)N(R⁸)R⁹ (worin n 1 bis 3 bedeutet), -O(CH₂)_pC(O)OR⁸ (worin p 1 bis 6 bedeutet), -N (R⁸) (CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (worin n jeweils unabhängig 1 bis 3 bedeutet), Morpholin-4-yl, 3-Tetrahydrofuranoxy,
oder Aryloxy (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus -OR⁸, -C(O)N(R⁸)R⁹, Halogen, Alkyl, Carboxy, Alkoxycarbonyl, Halogenalkoxy, Halogenalkoxycarbonyl, Alkoxycarbonylalkyl, Carboxyalkyl, Aminocarbonylalkyl, (Alkylamino)-carbonylalkyl, (Dialkylamino)carbonylalkyl, (Arylamino)carbonylalkyl, (Aralkylamino)-carbonylalkyl, Alkoxycarbonylalkenyl, Carboxyalkenyl, Aminocarbonylalkenyl, (Alkylamino)carbonylalkenyl, (Dialkyl-amino)carbonylalkenyl, (Arylamino)carbonylalkenyl, (Aralkylamino)carbonylalkenyl, (Hydroxyalkoxy)-carbonyl, (Alkoxy)alkoxycarbonyl, (Hydroxyalkoxy)-alkoxycarbonyl, ((Alkoxy)alkoxy)alkoxycarbonyl, Tetrazolyl, Morpholin-4-ylalkyl und (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl), ausgewählte Substituenten),
oder Piperazin-1-yl (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus Alkyl, Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl, ausgewählte Substituenten),
oder 1-Piperazinoyl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder Piperidin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder (3,4)-Piperidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkylcarbonyl, Carboxy, -C(O)N (R⁸)R⁹, Alkoxycarbonyl, Carboxyalkyl, Alkoxycarbonylalkyl und Tetrazolylalkyl),
oder Piperidin-4-ylamino (worin die Aminogruppe gegebenenfalls durch Alkyl substituiert ist und die Piperidinylgruppe gegebenenfalls durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Alkoxycarbonyl, Carboxyalkyl, -C(O)N(R⁸)R⁹, Alkoxycarbonylalkyl und Aralkyl substituiert ist),
oder 3-Pyrrolidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Aralkyl, Amidino, 1-Iminoethyl, Carboxy, Carboxyalkyl, -C (O)N(R⁸)R⁹, Alkoxycarbonyl und Alkoxycarbonylalkyl) steht;

R⁴ und R⁷ unabhängig voneinander für Wasserstoff, Halogen, Alkyl, Nitro, -OR⁸, -C(O)OR⁸, -C(O)N(R⁸) R⁹, -N(R⁸)R⁹, -N(H)C(O)R⁸ oder -N(H)S(O)₂R¹² stehen;

R⁵ für -C(NH)NH₂, -C(NH)N(H)OR⁸, -C (NH) N (H)C(O)OR¹², -C(NH)N(H)S(O)₂R¹², -C(NH)N(H)C(O)N(R⁸)R⁹ oder -C(NH)N(H)C(O)R⁸ steht;

R⁶ für Halogen, Alkyl, Halogenalkyl, Halogenalkoxy, Nitro, Amino, Ureido, Guanidino, -OR⁸, -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH2)_mC(O)N(R⁸)R⁹ (worin m 0 bis 3 bedeutet), -CH (OH)C (O)N (R⁸) R⁹, -(CH₂)_mN (R⁸) R⁹ (worin m 0 bis 3 bedeutet), -(CH₂)_mC(O)OR⁸ (worin m 0 bis 3 bedeutet), -N(H)C(O)R⁸, (1,2)-Tetrahydropyrimidinyl (gegebenenfalls substituiert durch Alkyl), (1,2)-Imidazolyl (gegebenenfalls substituiert durch Alkyl) oder (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl) steht;

R⁸ und R⁹ jeweils unabhängig voneinander für Wasserstoff, Alkyl, Aryl oder Aralkyl stehen;

R¹⁰ für Wasserstoff, Alkyl, Aryl, Aralkyl, 1-Pyrrolidinyl, 4-Morpholinyl, 4-Piperazinyl, 4-(N-Methyl)piperazinyl oder Piperidin-1-yl steht;

R¹¹ für Wasserstoff, Alkyl oder Halogen steht und

R¹² für Alkyl, Aryl oder Aralkyl steht;
oder ein pharmazeutisch unbedenkliches Salz davon, mit der Maßgabe, daß in dem Fall, daß die Verbindung der Formel IV entspricht und R⁵ und R⁶ beide für -C(NH)NH₂ stehen, gleichzeitig weder Z¹ noch Z² für -O- oder -N (R⁸)-, worin R⁸ H bedeutet, stehen und

R² nicht für H, -N (R⁸) R⁹, worin R⁸ und R⁹ H, -CH₃ oder -C₂H₅ bedeutet, oder -OR⁸, worin R⁸ -CH₃ bedeutet, steht;

und wobei "Alkyl" sich auf C₁-C₆-Alkyl bezieht.

2. Verbindung der Formel (I):

worin

A für -N= steht;

Z¹ und Z² unabhängig voneinander für -O-, -N(R⁸)-oder -OCH₂- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor, Chlor, Halogenalkyl, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N (R⁸) C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, oder -N(R⁸)S(O)₂R¹² stehen;

R² für Wasserstoff, Halogen, Alkyl, Halogenalkoxy, -OR⁸, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (worin m 0 bis 3 bedeutet), -N (R⁸) (CH₂)_nC(O)OR⁸ (worin n 1 bis 3 bedeutet), -N ((CH₂)_nN(R⁸)R⁹) (CH₂)_nC(O)OR⁸ (worin n jeweils 1 bis 3 bedeutet), -O(CH₂)_nC(O)N(R⁸)R⁹ (worin n 1 bis 3 bedeutet), -O(CH₂)_pC(O)OR⁸ (worin p 1 bis 6 bedeutet), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (worin n jeweils unabhängig 1 bis 3 bedeutet), Morpholin-4-yl, 3-Tetrahydrofuranoxy,
oder Aryloxy (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus -OR⁸, -C(O)N(R⁸)R⁹, Halogen, Alkyl, Carboxy, Alkoxycarbonyl, Halogenalkoxy, Halogenalkoxycarbonyl, Alkoxycarbonylalkyl, Carboxyalkyl, Aminocarbonylalkyl, (Alkylamino)carbonylalkyl, (Dialkylamino)-carbonylalkyl, (Arylamino)carbonylalkyl, (Aralkylamino)carbonylalkyl, Alkoxycarbonylalkenyl, Carboxyalkenyl, Aminocarbonylalkenyl, (Alkylamino)carbonylalkenyl, (Dialkylamino) carbonylalkenyl, (Arylamino)carbonylalkenyl, (Aralkylamino)carbonylalkenyl, (Hydroxyalkoxy)-carbonyl, (Alkoxy)alkoxycarbonyl, (Hydroxyalkoxy)-alkoxycarbonyl, ((Alkoxy)alkoxy)alkoxycarbonyl, Tetrazolyl, Morpholin-4-ylalkyl und (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl), ausgewählte Substituenten),
oder Piperazin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Carboxy, -C (O) N (R⁸) R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder 1-Piperazinoyl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Carboxy, -C (O) N (R⁸) R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder Piperidin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder (3,4)-Piperidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkylcarbonyl, Carboxy, -C(O)N(R⁸)R⁹, Alkoxycarbonyl, Carboxyalkyl, Alkoxycarbonylalkyl und Tetrazolylalkyl),
oder Piperidin-4-ylamino (worin die Aminogruppe gegebenenfalls durch Alkyl substituiert ist und die Piperidinylgruppe gegebenenfalls durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Alkoxycarbonyl, Carboxyalkyl, -C(O)N(R⁸)R⁹, Alkoxycarbonylalkyl und Aralkyl substituiert ist),
oder 3-Pyrrolidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Aralkyl, Amidino, 1-Iminoethyl, Carboxy, Carboxyalkyl, -C(O)N(R⁸)R⁹, Alkoxycarbonyl und Alkoxycarbonylalkyl) steht;

R⁴ für Wasserstoff, -OR⁸ oder -N (R⁸) R⁹ steht;

R⁵ für -C(NH)NH₂ steht;

R⁶ für Guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (worin m 0 bis 3 bedeutet), 1-Piperidinoyl, 1-Pyrrolidinoyl, (1,2)-Imidazolyl (gegebenenfalls substituiert durch Alkyl) oder (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl) steht;

R⁷ für Wasserstoff, Halogen, Alkyl, -OR⁸ oder -C(O)N(R⁸)R⁹ steht;

R⁸ und R⁹ jeweils unabhängig voneinander für Wasserstoff, Methyl, Ethyl oder Phenyl stehen und R¹² für Methyl, Ethyl, Phenyl oder Benzyl steht.

3. Verbindung nach Anspruch 2, worin

Z¹ und Z² unabhängig voneinander für -O- oder -NCH₃- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor, Chlor, Trifluormethyl, Amino, -C(O)N(R⁸)R⁹ oder -NHC(O)NHR⁹ stehen;

R² für Wasserstoff, Halogen, Alkyl, Halogenalkoxy, -OR⁸, -C(O)OR⁸, -N(R⁸)R⁹_, -N(R⁸)(CH₂)_nC(O)OR⁸ (worin n 1 bis 3 bedeutet), -N((CH₂)_nN(R⁸)R⁹) (CH_z)_nC(O) OR⁸ (worin n jeweils 1 bis 3 bedeutet), -O(CH₂)_nC(O)N(R⁸)R⁹ (worin n 1 bis 3 bedeutet), -O(CH₂)_pC(O)OR⁸ (worin p 1 bis 6 bedeutet), -N(R⁸) (CH₂)_nC(O)N(R⁸) (CH₂)_nC(O)OR⁸ (worin n jeweils unabhängig 1 bis 3 bedeutet), Morpholin-4-yl, 3-Tetrahydrofuranoxy,
oder Aryloxy (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus -OR⁸, -C (O) N (R⁸) R⁹, Halogen, Alkyl, Carboxy, Alkoxycarbonyl, Alkoxycarbonylalkyl, Carboxyalkyl, Alkoxycarbonylalkenyl, Carboxyalkenyl, Tetrazolyl, Morpholin-4-ylalkyl und (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl), ausgewählte Substituenten),
oder Piperazin-1-yl (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus Alkyl, Carboxyalkyl und Alkoxycarbonylalkyl, ausgewählte Substituenten),
oder Piperidin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxy und Alkoxycarbonyl),
oder (3,4)-Piperidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxyalkyl und Alkoxycarbonylalkyl),
oder Piperidin-4-ylamino (worin die Aminogruppe gegebenenfalls durch Alkyl substituiert ist und die Piperidinylgruppe gegebenenfalls durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxyalkyl, Alkoxycarbonylalkyl und Aralkyl substituiert ist),
oder 3-Pyrrolidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus 1-Iminoethyl, Carboxy, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl) steht;

R⁴ für Wasserstoff, Amino, Hydroxy oder Methoxy steht;

R⁵ für -C(NH)NH₂ steht;

R⁶ für Guanidino, -C (NH) NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (worin m 0 bis 1 bedeutet), durch Alkyl substituiertes (1,2)-Imidazolyl oder durch Alkyl substituiertes 2-Imidazolinyl steht;

R⁷ für Wasserstoff, Methoxy oder Hydroxy steht und

R⁸ und R⁹ jeweils unabhängig voneinander für Wasserstoff, Methyl, Ethyl oder Phenyl stehen.

4. Verbindung nach Anspruch 3, worin

Z¹ und Z² beide für -O- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor oder Chlor stehen;

R⁴ für Amino, Wasserstoff, Hydroxy oder Methoxy steht;

R⁶ für Guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (worin m 0 bis 1 bedeutet), durch Methyl substituiertes (1,2)-Imidazolyl oder gegebenenfalls durch Methyl substituiertes 2-Imidazolinyl steht und

R⁷ für Wasserstoff oder Hydroxy steht.

5. Verbindung nach Anspruch 4, worin

R⁴ für Hydroxy steht;

R⁶ für Dimethylamino oder Dimethylaminocarbonyl steht und

R⁷ für Wasserstoff steht.

6. Verbindung nach Anspruch 5 aus der Gruppe bestehend aus:

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(2-methoxy-4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-propoxypyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxypiperidin-1-yl)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-dimethylaminopyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(2,2,2-trifluorethoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(l,3-difluorprop-2-oxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(1-brom-3-fluorprop-2-oxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-methylpyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-((methyl)(carboxymethyl)amino)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-methoxypyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(4-carboxymethylpiperazin-1yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(piperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(4-methylpiperazin-1-yl)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(morpholin-4-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(4-carboxymethylpiperazinyl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(4-ethoxycarbonylmethylpiperazinyl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-methoxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(4-carboxy-2-(morpholin-4-ylmethyl)phenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-((methyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(aminocarbonylmethoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)pyridin-2-yl)oxy] benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-carboxymethoxypyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-((2-dimethylaminoethyl)-(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(1-ethoxycarbonylmethylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-(1-(1-iminoethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-4-((1-carboxymethyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin und

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminophenoxy)-4-((methyl)((carboxymethyl)aminocarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidin;

7. Verbindung nach Anspruch 4, worin

R⁴ für Hydroxy steht;

R⁶ für durch Methyl substituiertes (1,2)-Imidazolyl oder durch Methyl substituiertes 2-Imidazolinyl steht und

R⁷ für Wasserstoff steht.

8. Verbindung nach Anspruch 7 aus der Gruppe bestehend aus:

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3- (1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-4-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((methyl)(ethoxycarbonylmethyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-(methoxycarbonyl)ethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-(ethoxycarbonyl)ethenyl)phenoxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-(2-carboxyethenyl)phenoxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(1-ethoxycarbonyl)-ethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[ (3,5-difluor-6-(3-(1methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin; 4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,3-dimethoxy-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin; 4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(1-methylimidazolin-2-yl)phenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3,5-dicarboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-4-(3-(1-methylimidazolin-2-yl)phenoxy)-6-(3,5-dicarboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxy-5-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-hydroxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-amidinophenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-aminocarbonyl-5-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-chlor-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2,6-dimethyl-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-(ethoxycarbonylmethyl)piperazin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(1-(1-carboxy-1-methylethyl)piperidin-4-yloxy)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-ethoxycarbonylpiperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-carboxypiperidin-1-yl)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxypiperidin-1-yl)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(3-(2-ethoxycarbonylethyl)phenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-ethoxycarbonylmethylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-4-carboxymethylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(2-methoxy-5-(tetrazol-5-yl)phenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazol-2-yl)phenoxy)-4-((2-dimethylaminoethyl)(carboxymethyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-carboxymethylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)-oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-ethoxycarbonylmethyl)piperidin-4-yl)amino)pyridin-2-yl)oxy]-benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((piperidin-4-yl)-amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((piperidin-4-yl)-(methyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-((1-benzylpiperidin-4-yl)(methyl)amino)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(5-carboxypent-1-oxy)-pyridin-2-yl)oxy]benzamidin und

4-Hydroxy-3-[(3,5-difluor-6-(3-(1-methylimidazolin-2-yl)phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidin.

9. Verbindung nach Anspruch 4, worin

R⁴ für Hydroxy steht;

R⁶ für Guanidino steht und

R⁷ für Wasserstoff steht.

10. Verbindung nach Anspruch 9 aus der Gruppe bestehend aus:

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(1-ethoxycarbonylmethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(1-carboxymethylpiperidin-4-yloxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(5-ethoxycarbonylpyrrolidin-3-yloxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(2,6-dimethoxy-4-methoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(2,6-dimethoxy-4-ethoxycarbonylphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(2,6-dimethoxy-4-carboxyphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(2,6-dimethoxy-4-aminocarbonylphenoxy)-pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(2-methoxy-4-carboxyphenoxy)pyridin-2-yl)oxy]benzamidin;

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(methyl)(phenyl)aminocarbonylpyridin-2-yl)oxy]benzamidin und

4-Hydroxy-3-[(3,5-difluor-6-(3-(guanidino)-phenoxy)-4-(4-carboxymethylpiperazin-1-yl)pyridin-2-yl)oxy]benzamidin.

11. Verbindung nach Anspruch 1 der Formel (VII):

worin

Z¹ und Z² unabhängig voneinander für -O-, -N(R⁸)-oder -OCH₂- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor, Chlor, Halogenalkyl, -N (R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N (R⁸)C(O)R⁸, oder -N(R⁸)S(O)₂R¹2 stehen;

R² für Wasserstoff, Halogen, Alkyl, Halogenalkoxy, - OR⁸, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N (R⁸)R⁹, -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (worin m 0 bis 3 bedeutet), -N(R⁸)(CH₂)_nC(O)OR⁸ (worin n 1 bis 3 bedeutet), -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)_nOR⁸ (worin n jeweils 1 bis 3 bedeutet), -C(CH₂)_nC(O)N(R⁸)R⁹ (worin n 1 bis 3 bedeutet), -O(CH₂)_pC(O)OR⁸ (worin p 1 bis 6 bedeutet), -N (R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (worin n jeweils unabhängig 1 bis 3 bedeutet), Morpholin-4-yl, 3-Tetrahydrofuranoxy,
oder Aryloxy (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus -OR⁸, -C(O)N(R⁸)R⁹, Halogen, Alkyl, Carboxy, Alkoxycarbonyl, Halogenalkoxy, Halogenalkoxycarbonyl, Alkoxycarbonylalkyl, Carboxyalkyl, Aminocarbonylalkyl, (Alkylamino)carbonylalkyl, (Dialkylamino)-carbonylalkyl, (Arylamino)carbonylalkyl, (Aralkylamino)carbonylalkyl, Alkoxycarbonylalkenyl, Carboxyalkenyl, Aminocarbonylalkenyl, (Alkylamino)carbonylalkenyl, (Dialkylamino)carbonylalkenyl, (Arylamino)carbonylalkenyl, (Aralkylamino)carbonylalkenyl, (Hydroxyalkoxy)-carbonyl, (Alkoxy)alkoxycarbonyl, (Hydroxyalkoxy)-alkoxycarbonyl, ((Alkoxy)alkoxy)alkoxycarbonyl, Tetrazolyl, Morpholin-4-ylalkyl und (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl), ausgewählte Substituenten), oder Piperazin-1-yl (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus Alkyl, Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl, ausgewählte Substituenten),
oder 1-Piperazinoyl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder Piperidin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxy, -C(O)N(R⁸)R⁹, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl),
oder (3,4)-Piperidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkylcarbonyl, Carboxy, -C(O)N(R⁸)R⁹, Alkoxycarbonyl, Carboxyalkyl, Alkoxycarbonylalkyl und Tetrazolylalkyl),
oder Piperidin-4-ylamino (worin die Aminogruppe gegebenenfalls durch Alkyl substituiert ist und die Piperidinylgruppe gegebenenfalls durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Alkoxycarbonyl, Carboxyalkyl, -C(O)N(R⁸)R⁹, Alkoxycarbonylalkyl und Aralkyl substituiert ist),
oder 3-Pyrrolidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Alkyl, Aralkyl, Amidino, 1-Iminoethyl, Carboxy, Carboxyalkyl, -C(O)N(R⁸)R⁹, Alkoxycarbonyl und Alkoxycarbonylalkyl) steht;

R⁴ für Wasserstoff, -OR⁸ oder -N (R⁸)R⁹ steht;

R⁵ für -C(NH)NH₂ steht;

R⁶ für Guanidino, -C(NH)NH₂, -C(O)N (R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (worin m 0 bis 3 bedeutet), 1-Piperidinoyl, 1-Pyrrolidinoyl, (1,2)-Imidazolyl (gegebenenfalls substituiert durch Alkyl) oder (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl) steht;

R⁷ für Wasserstoff, Halogen, Alkyl, -OR⁸ oder -C(O)N(R⁸)R⁹ steht;

R⁸ und R⁹ unabhängig voneinander für Wasserstoff, Methyl, Ethyl oder Phenyl stehen und

R¹² für Methyl, Ethyl, Phenyl oder Benzyl steht.

12. Verbindung nach Anspruch 11, worin

Z¹ und Z² unabhängig voneinander für -O- oder - NCH₃- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor, Chlor, Trifluormethyl, Amino, -C(O)N(R⁸)R⁹ oder -NHC(O)NHR⁹ stehen;

R² für Wasserstoff, Halogen, Alkyl, Halogenalkoxy, -OR⁸, -C(O)OR⁸, -N (R⁸)R⁹, -N (R⁸)(CH₂)_nC(O)OR⁸ (worin n 1 bis 3 bedeutet), -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (worin n jeweils 1 bis 3 bedeutet), -O(CH₂)_nC(O)N(R⁸)R⁹ (worin n 1 bis 3 bedeutet), -O(CH₂)_pC(O)OR⁸ (worin p 1 bis 6 bedeutet), -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (worin n jeweils 1 bis 3 bedeutet), Morpholin-4-yl, 3-Tetrahydrofuranoxy,
oder Aryloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus -OR⁸, -C(O)N(R⁸)R⁹, Halogen, Alkyl, Carboxy, Alkoxycarbonyl, Alkoxycarbonylalkyl, Carboxyalkyl, Alkoxycarbonylalkenyl, Carboxyalkenyl, Tetrazolyl, Morpholin-4-ylalkyl und (1,2)-Imidazolinyl (gegebenenfalls substituiert durch Alkyl)),
oder Piperazin-1-yl (gegebenenfalls substituiert durch einen oder mehrere, unabhängig voneinander aus der Gruppe bestehend aus Alkyl, Carboxyalkyl und Alkoxycarbonylalkyl, ausgewählte Substituenten),
oder Piperidin-1-yl (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxy und Alkoxycarbonyl),
oder (3,4)-Piperidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxyalkyl und Alkoxycarbonylalkyl),
oder Piperidin-4-ylamino (worin die Aminogruppe gegebenenfalls durch Alkyl substituiert ist und die Piperidinylgruppe gegebenenfalls durch einen oder mehrere Substituenten aus der Gruppe bestehend aus Carboxyalkyl, Alkoxycarbonylalkyl und Aralkyl substituiert ist),
oder 3-Pyrrolidinyloxy (gegebenenfalls substituiert durch einen oder mehrere Substituenten aus der Gruppe bestehend aus 1-Iminoethyl, Carboxy, Carboxyalkyl, Alkoxycarbonyl und Alkoxycarbonylalkyl) steht;

R⁴ für Wasserstoff, Amino, Hydroxy oder Methoxy steht;

R⁵ für -C(NH)NH₂ steht;

R⁶ für Guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (worin m 0 bis 1 bedeutet), durch Alkyl substituiertes (1,2)-Imidazolyl oder durch Alkyl substituiertes 2-Imidazolinyl steht;

R⁷ für Wasserstoff, Methoxy oder Hydroxy steht und

R⁸ und R⁹ jeweils unabhängig voneinander für Wasserstoff, Methyl, Ethyl oder Phenyl stehen.

13. Verbindung nach Anspruch 12, worin

Z¹ und Z² beide für -O- stehen;

R¹ und R³ unabhängig voneinander für Wasserstoff, Fluor oder Chlor stehen;

R⁴ für Amino, Wasserstoff, Hydroxy oder Methoxy steht;

R⁶ für Guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (worin m 0 bis 1 bedeutet), durch Methyl substituiertes (1,2)-Imidazolyl oder gegebenenfalls durch Methyl substituiertes 2-Imidazolinyl steht und

R⁷ für Wasserstoff oder Hydroxy steht.

14. Verbindung nach Anspruch 13, worin

R⁴ für Hydroxy steht;

R⁶ für Dimethylamino oder Dimethylaminocarbonyl steht und

R⁷ für Wasserstoff steht.

15. Verbindung nach Anspruch 14 aus der Gruppe bestehend aus:

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-2-methoxypyridin-4-yl)oxy]-benzamidin und

4-Hydroxy-3-[(3,5-difluor-6-(3-dimethylaminocarbonylphenoxy)-2-(2-methoxy-5-ethoxycarbonylphenoxy)pyridin-4-yl)oxy]benzamidin.

16. Pharmazeutische Zusammensetzung, die zur Verwendung bei der Behandlung eines Menschen, der sich in einem durch thrombotische Aktivität gekennzeichneten Krankheitszustand befindet, geeignet ist und eine therapeutisch wirksame Menge einer Verbindung nach einem der vorhergehenden Ansprüche enthält.

17. Verwendung einer therapeutisch wirksamen Menge einer Verbindung nach einem der Ansprüche 1 bis 15 zur Herstellung eines Arzneimittels zur Behandlung eines durch thrombotische Aktivität gekennzeichneten Krankheitszustands.

18. Verbindung nach einem der Ansprüche 1 bis 15 zur Verwendung als Arzneimittel.

19. Verwendung nach Anspruch 17, bei der es sich bei dem Arzneimittel um ein Antikoagulans handelt.

20. Verwendung nach Anspruch 17 oder 19, bei der die Behandlung die Prophylaxe für das Langzeitrisiko nach Herzinfarkt, die Prophylaxe von tiefer Venenthrombose (DVT) nach orthopädischen Eingriffen, die Prophylaxe bei ausgewählten Patienten nach einem vorübergehenden ischämischen Anfall; die Behandlung von tiefer Venenthrombose (DVT); die Behandlung in Verbindung mit chirurgischen Eingriffen wie dem Legen eines Bypasses an der Koronararterie und perkutaner transluminaler Koronarangioplastie; die Behandlung von thrombotischen Komplikationen in Verbindung mit akuter promyelozytärer Leukämie, Diabetes, multiplen Myelomen, disseminierter intravasaler Koagulation in Assoziation mit septischem Schock, Infektionen in Verbindung mit Purpura fulminans, Schocklunge, instabiler Angina und thrombotischen Komplikationen in Verbindung mit Aortenklappenoder Gefäßprothesen; die Prophylaxe für thrombotische Krankheiten, insbesondere bei Patienten mit hohem Erkrankungsrisiko, beinhaltet.

Revendications

1. Composition choisie parmi le groupe constitué des formules suivantes :







dans lesquelles

A   est -N= ;

Z¹ et Z²   sont indépendamment -O-, -N(R⁸)-, -S- ou -OCH₂- ;

R¹   et R³ sont indépendamment un hydrogène, un halogéno, un alkyle, un halogénoalkyle, un alcoxy, un halogénoalcoxy, un nitro, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, -N(R⁸)S(O)₂R¹² ou -N(R⁸)C(O)N(R⁸)CH₂C(O)N(R⁸)R⁹ ;

R²   est un hydrogène ; un halogéno ; un alkyle ; un halogénoalcoxy ; -OR⁸ ; -C(O)OR⁸ ; -C(O)N(R⁸)R⁹; -N(R⁸)R⁹; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (où m vaut de 0 à 3) ; -N(R⁸)(CH₂)_nC(O)OR⁸ (où n vaut de 1 à 3) ; -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (où chaque n vaut de 1 à 3) ; -O(CH₂)_nC(O)N(R⁸)R⁹ (où n vaut de 1 à 3) ; -O(CH₂)_pC(O)OR⁸ (où p vaut de 1 à 6) ; -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (où chaque n vaut indépendamment de 1 à 3) ; un morpholin-4-yle ; un 3-tétrahydrofuranoxy ;
ou R² est un aryloxy (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué de -OR⁸, de -C(O)N(R⁸)R⁹, d'un halogéno, d'un alkyle, d'un carboxy, d'un alcoxycarbonyle, d'un halogénalcoxy, d'un halogénoalcoxy-carbonyle, d'un alcoxycarbonylalkyle, d'un carboxyalkyle, d'un aminocarbonylalkyle, d'un (alkylamino)carbonylalkyle, d'un (dialkyl-amino)carbonylalkyle, d'un (arylamino)carbonyl-alkyle, d'un (aralkylamino)carbonylalkyle, d'un alcoxycarbonylalcényle, d'un carboxyalcényle, d'un aminocarbonylalcényle, d'un (alkylamino)-carbonylalcényle, d'un (dialkylamino)-carbonylalcényle, d'un (arylamino)-carbonylalcényle, d'un (aralkylamino)-carbonylalcényle, d'un (hydroxyalcoxy)-carbonyle, d'un (alcoxy)alcoxycarbonyle, d'un (hydroxyalcoxy)alcoxycarbonyle, d'un ((alcoxy)-alcoxy)alcoxycarbonyle, d'un tétrazolyle, d'un morpholin-4-ylalkyle et d'un (1,2)-imidazolinyle (éventuellement substitué par un alkyle)) ;
ou R² est un pipérazin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un 1-pipérazinoyle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle) ;
ou R² est un pipéridin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un (3,4)-pipéridinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkylcarbonyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle, d'un carboxyalkyle, d'un alcoxycarbonylalkyle et d'un tétrazolylalkyle) ;
ou R² est un pipéridin-4-ylamino (dans lequel l'amino est éventuellement substitué par un alkyle et le groupe pipéridinyle est éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un alcoxycarbonyle, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonylalkyle et d'un aralkyke) ;
ou R² est un 3-pyrrolidinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un aralkyle, d'un amidino, d'un 1-iminoéthyle, d'un carboxy, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);

R⁴ et R⁷   sont indépendamment un hydrogène ; un halogéno, un alkyle, un nitro, -OR⁸, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)R⁹, -N(H)C(O)R⁸ ou -N(H)S(O)₂R¹² ;

R⁵   est -C(NH)NH₂, -C(NH)N(H)OR⁸, -C(NH)N(H)C(O)OR¹², -C(NH)N(H)S(O)₂R¹², C(NH)N(H)C(O)N(R⁸)R⁹ ou -C(NH)N(H)C(O)R⁸ ;

R⁶   est un halogéno, un alkyle, un halogénoalkyle, un halogénoalcoxy, un nitro, un amino, un uréido, un guanidino, -OR⁹, -C(NH)NH₂, -C(NH)NHOH, -C(O)R¹⁰, -(CH₂)_mC O)N(R⁸)R⁹ (où m vaut de 0 à 3), -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (où m vaut de 0 à 3), (CH₂)_mC(O)OR⁸ (où m vaut de 0 à 3), -N(H)C(O)R⁸, un (1,2)-tétrahydropyrimidinyle (éventuellement substitué par un alkyle), un (1,2)-imidazolyle (éventuellement substitué par un alkyle) ou un (1,2)-imidazolinyle (éventuellement substitué par un alkyle) ;
chaque R⁸ et chaque R⁹ sont indépendamment un hydrogène, un alkyle, un aryle ou un aralkyle ;

R¹⁰   est un hydrogène, un alkyle, un aryle, un aralkyle, un 1-pyrrolidinyle, un 4-morpholinyle, un 4-pipérazinyle, un 4-(N-méthyl)pipérazinyle ou un pipéridin-1-yle ;

R¹¹   est un hydrogène, un alkyle ou un halogéno ; et

R¹²   est un alkyle, un aryle ou un aralkyle ;

ou un sel pharmaceutiquement acceptable de celui-ci,
à condition que lorsque le composé est choisi parmi la formule IV, et R⁵ et R⁶ sont tous les deux -C(NH)NH₂, simultanément
   à la fois Z¹ et Z² ne soient pas -O- ou -N(R⁸)-, où R⁸ est H ; et
   R² ne soit pas H ; -N(R⁸)R⁹ où R⁸ et R⁹ sont H, -CH₃ ou -CH₂CH₃ ; ou -OR⁸ où R⁸ est -CH₃ ;
   et où le terme "alkyle" désigne un alkyle en C₁-C₆.

2. Composé choisi parmi la formule (I) :

dans laquelle

A   est -N= ;

Z¹ et Z²   sont indépendamment -O-, -N(R⁸)- ou -OCH₂- ;

R¹ et R³   sont indépendamment un hydrogène, un fluoro, un chloro, un halogénoalkyle, -N(R8)R9, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, ou -N(R⁸)S(O)₂R¹²;

R²   est un hydrogène ; un halogéno ; un alkyle ; un halogénoalcoxy ; -OR⁸ ; -C(O)OR⁸; -C(O)N(R⁸)R⁹; -N(R⁸)R⁹ ; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (où m vaut de 0 à 3) ; -N(R⁸)(CH₂)_nC(O)OR⁸ (où n vaut de 1 à 3) ; -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (où chaque n vaut de 1 à 3) ; -O(CH₂)_nC(O)N(R⁸)R⁹ (où n vaut de 1 à 3) ; -O(CH₂)_pC(O)OR⁸ (où p vaut de 1 à 6) ; -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (où chaque n vaut indépendamment de 1 à 3) ; un morpholin-4-yle ; un 3-tétrahydrofuranoxy ;
ou R² est un aryloxy (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué de -OR⁸, de -C(O)N(R⁸)R⁹, d'un halogéno, d'un alkyle, d'un carboxy, d'un alcoxycarbonyle, d'un halogénalcoxy, d'un halogénoalcoxycarbonyle, d'un alcoxycarbonylalkyle, d'un carboxyalkyle, d'un aminocarbonylalkyle, d'un (alkylamino)carbonylalkyle, d'un (dialkylamino)carbonylalkyle, d'un (arylamino)carbonylalkyle, d'un (aralkylamino)carbonylalkyle, d'un alcoxycarbonylalcényle, d'un carboxyalcényle, d'un aminocarbonylalcényle, d'un (alkylamino)carbonylalcényle, d'un (dialkylamino)carbonylalcényle, d'un (arylamino)carbonylalcényle, d'un (aralkylamino)carbonylalcényle, d'un (hydroxyalcoxy)carbonyle, d'un (alcoxy)alcoxycarbonyle, d'un (hydroxyalcoxy)alcoxycarbonyle, d'un ((alcoxy)alcoxy)alcoxycarbonyle, d'un tétrazolyle, d'un morpholin-4-ylalkyle et d'un (1,2)imidazolinyle (éventuellement substitué par un alkyle)) ;
ou R² est un pipérazin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un 1-pipérazinoyle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle) ;
ou R² est un (3,4)-pipéridinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkylcarbonyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle, d'un carboxyalkyle, d'un alcoxycarbonylalkyle ou d'un tétrazolyl-alkyle) ;
ou R² est un pipéridin-4-ylamino (dans lequel l'amino est éventuellement substitué par un alkyle et le groupe pipéridinyle est éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un alcoxycarbonyle, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonylalkyle et d'un aralkyke) ;
ou R² est un 3-pyrrolidinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un aralkyle, d'un amidino, d'un 1-iminoéthyle, d'un carboxy, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);

R⁴   est un hydrogène, -OR ou -N(R⁸)R⁹ ;

R⁵   est -C(NH)NH₂

R⁶   est un guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹,(CH₂)_mN(R⁸)R⁹ (où m vaut de 0 à 3), un 1-pipéridinoyle, un 1-pyrrolidinoyle, un (1,2)-imidazolyle (éventuellement substitué par un alkyle) ou un (1,2)-imidazolinyle (éventuellement substitué par un alkyle) ;

R⁷   est un hydrogène, un halogéno, un alkyle, -OR⁸, -C(O)N(R⁸)R⁹;

R⁸   et R⁹ sont indépendamment un hydrogène, un méthyle, un éthyle ou un phényle ; et

R¹²   est un méthyle, un éthyle, un phényle ou un benzyle.

3. Composé selon la revendication 2, dans lequel

Z¹ et Z²   sont indépendamment -O- ou -NCH₃- ;

R¹ et R³   sont indépendamment un hydrogène, un fluoro, un chloro, un trifluorométhyle, un amino, -C(O)N(R⁸)R⁹ ou -NHC(O)NHR⁹

R²   est un hydrogène, un halogéno, un alkyle, un halogénoalcoxy ; -OR⁸ ; -C(O)OR⁸ ; -N(R⁸)R⁹ ; -N (R⁸)(CH₂)_nC(O)OR⁸ (où n vaut de 1 à 3) ; -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (où chaque n vaut de 1 à 3) ; O(CH₂)_nC(O)N(R⁸)R⁹ (où n vaut de 1 à 3) ; -O(CH₂)_pC(O)OR⁸ (où p vaut de 1 à 6) ; -N (R⁸)(CH₂)_nC(O)N(R⁸) (CH₂)_nC(O)OR⁸ (où chaque n vaut indépendamment de 1 à 3) ; un morpholin-4-yle ; un 3-tétrahydrofuranoxy ;
ou R² est un aryloxy (éventuellement substitué par un ou plusieurs substituants choisi indépendamment parmi le groupe constitué de -OR⁸, -C(O)N(R⁸)R⁹, d'un halogéno, d'un alkyle, d'un carboxy, d'un alcoxycarbonyle, d'un alcoxycarbonylalkyle, d'un carboxyalkyle, d'un alcoxycarbonylalcényle, d'un carboxyalcényle, d'un tétrazolyle, d'un morpholin-4-ylalkyle et d'un (1,2)-imidazolinyle (éventuellement substitué par un alkyle)) ;
ou R² est un pipérazin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué d'un alkyle, d'un carboxyalkyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxy et d'un alcoxycarbonyle) ;
ou R² est un (3,4)-pipéridinyloxy (éventuellement substitué par un ou plusieurs substituants carboxyalkyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-4-ylamino (où l'amino est éventuellement substitué par un alkyle et le groupe pipéridinyle est éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxyalkyle, d'un alcoxycarbonylalkyle et d'un aralkyle) ;
ou R² est un 3-pyrrolidinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un 1-iminoéthyle, d'un carboxy, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);

R⁴   est un hydrogène, un amino, un hydroxy ou un méthoxy ;

R⁵   est -C(NH)NH₂ ;

R⁶   est un guanidino, -C(NH)NH₂, -C (O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (où m vaut de 0 à 1) , un (1,2)-imidazolyle substitué par un alkyle ou un 2-imidazolinyle substitué par un alkyle ;

R⁷   est un hydrogène, un méthoxy ou un hydroxy ; et

R⁸ et R⁹   sont indépendamment un hydrogène, un méthyle, un éthyle ou un phényle.

4. Composé selon la revendication 3, dans lequel

Z¹ et Z²   sont tous les deux -O- ;

R¹ et R³   sont indépendamment un hydrogène, un fluoro ou un chloro ;

R⁴   est un amino, un hydrogène, un hydroxy ou un méthoxy ;

R⁶   est un guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, (CH₂)_mN(R⁸)R⁹ (où m vaut 0 ou 1), un (1,2)-imidazolyle substitué par un méthyle ou un 2-imidazolinyle éventuellement substitué par un méthyle ; et

R⁷   est un hydrogène ou un hydroxy.

5. Composé selon la revendication 4, dans lequel

R⁴   est un hydroxy ;

R⁶   est un diméthylamino ou un diméthylamino-carbonyle ; et

R⁷   est un hydrogène.

6. Composé selon la revendication 5, choisi parmi le groupe constitué des composés suivants :

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(2-méthoxy-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(1-éthoxycarbonylméthylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-propoxypyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(4-carboxypipéridin-1-yl)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-diméthylaminopyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(2,2,2-trifluoréthoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(1,3-difluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(1-bromo-3-fluoroprop-2-oxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-méthylpyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-((méthyl)(carboxyméthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-méthoxypyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(3-carboxypipéridin-1-yl)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(4-carboxyméthylpipérazin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(pipéridin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(4-méthylpipérazin-1-yl)-pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(morpholin-4-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(4-carboxyméthylpipérazinyl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(4-éthoxycarbonylméthylpipérazinyl)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(4-carboxy-2-méthoxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(4-carboxy-2-(morpholin-4-ylméthyl)phénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-((méthyl)(carboxyméthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(aminocarbonylméthoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(1-carboxyméthylpipéridin-4-yloxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-carboxyméthoxypyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-((2-diméthylaminoéthyl)(carboxyméthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-(1-(1-iminoéthyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(1-éthoxycarbonylméthylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-(1-(1-iminoéthyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-4-((1-carboxyméthyl)pyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine; et

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminophénoxy)-4-((méthyl)((carboxyméthyl)aminocarbonylméthyl)amino)pyridin-2-yl)oxy]benzamidine.

7. Composé selon la revendication 4, dans lequel

R⁴   est un hydroxy ;

R⁶   est un (1,2)-imidazolyle substitué par un méthyle ou un 2-imidazolinyle substitué par un méthyle ; et

R⁷   est un hydrogène.

8. Composé selon la revendication 7, choisi parmi le groupe constitué des composés suivants :

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxycarbonylpipéridin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxyphénoxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-4-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((méthyl)(carboxyméthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((méthyl)(éthoxycarbonylméthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-(méthoxycarbonyl)éthylpipéridin-4-yl)amino)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,6-diméthoxy-4-(2-(éthoxycarbonyl)éthényl)phénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,6-diméthoxy-4-(2-carboxyéthényl)phénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(5-carboxypyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-(1-éthoxycarbonyl)-éthyl)pipérazin-1-yl)pyridin-2-yl]oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-4-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-hydroxy-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-carboxyphénoxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-5-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-5-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,3-diméthoxy-5-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,3-diméthoxy-5-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-aminocarbonyl-5-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-(1-méthylimidazolin-2-yl)phénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,6-diméthoxy-4-méthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,6-diméthoxy-4-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-carboxyphénoxy)-pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3,5-dicarboxyphénoxy)-pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-4-(3-(1-méthylimidazolin-2-yl)phénoxy)-6-(3,5-dicarboxyphénoxy)-pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[ (3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-carboxy-5-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2,6-diméthoxy-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-hydroxy-4-méthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-amidinophénoxy)-4-(2-méthoxy-4-carboxyphénoxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-aminocarbonyl-5-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-chloro-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2, 6-diméthyl-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-éthoxycarbonylméthyl)pipéridin-4-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-(éthoxycarbonylméthyl)pipérazin-1-yl)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(5-éthoxycarbonylpyrrolidin-3-yloxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(1-carboxyméthylpipéridin-4-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(1-(1-carboxy-1-méthyléthyl)pipéridin-4-yloxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-éthoxycarbonylpipéridin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-éthoxycarbonylpipéridin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-carboxypipéridin-1-yl)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-carboxypipéridin-1-yl)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(3-(2-éthoxycarbonyléthyl)phénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-4-éthoxycarbonylméthylphénoxy)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-4-carboxyméthylphénoxy)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(2-méthoxy-5-(tétrazol-5-yl)phénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazol-2-yl)phénoxy)-4-((2-diméthylaminoéthyl)-(carboxyméthyl)amino)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-carboxyméthylpipéridin-4-yl)(méthyl)amino)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-carboxyméthylpipéridin-4-yl)amino)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-éthoxycarbonylméthylpipéridin-4-yl)(méthyl)amino)pyridin-2-yl)-oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-éthoxycarbonylméthyl)pipéridin-4-yl)amino)pyridin-2-yl)oxy]-benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((pipéridin-4-yl)-amino)pyridin-2-yl)oxy]benzamidine;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-benzylpipéridin-4-yl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((pipéridin-4-yl)-(méthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-((1-benzylpipéridin-4-yl)(méthyl)amino)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(5-carboxypent-1-oxy)-pyridin-2-yl)oxy]benzamidine; et

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(1-méthylimidazolin-2-yl)phénoxy)-4-(4-carboxyméthylpipérazin-1-yl)pyridin-2-yl)oxy]benzamidine.

9. Composé selon la revendication 4, dans lequel

R⁴   est un hydroxy ;

R⁶   est un guanidino ; et

R⁷   est un hydrogène.

10. Composé selon la revendication 9, choisi parmi le groupe constitué des composés suivants :

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(1-éthoxycarbonylméthylpipéridin-4-yloxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(1-carboxyméthylpipéridin-4-yloxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(5-éthoxycarbonylpyrrolidin-3-yloxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(2,6-diméthoxy-4-méthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(2,6-diméthoxy-4-éthoxycarbonylphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(2,6-diméthoxy-4-carboxyphénoxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(2,6-diméthoxy-4-aminocarbonylphénoxy)-pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(2-méthoxy-4-carboxyphénoxy)pyridin-2-yl)oxy]benzamidine ;

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(méthyl)(phényl)aminocarbonylpyridin-2-yl)oxy]benzamidine ; et

la 4-hydroxy-3-[(3,5-difluoro-6-(3-(guanidino)-phénoxy)-4-(4-carboxyméthylpipérazin-1-yl)pyridin-2-yl)oxy]benzamidine.

11. Composé selon la revendication 1, qui est choisi parmi la formule (VII) :

dans laquelle

Z¹   et Z² sont indépendamment -O-, -N(R⁸)- ou -OCH₂- ;

R¹   et R³ sont indépendamment un hydrogène, un fluoro, un chloro, un halogénoalkyle, -N(R⁸)R⁹, -C(O)OR⁸, -C(O)N(R⁸)R⁹, -N(R⁸)C(O)N(R⁸)R⁹, -N(R⁸)C(O)R⁸, ou -N(R⁸)S(O)₂R¹² ;

R²   est un hydrogène ; un halogéno ; un alkyle ; un halogénoalcoxy ; -OR⁸ ; -C(O)OR⁸ ; -C(O)N(R⁸)R⁹ ; -N(R⁸)R⁹ ; -C(O)N(R⁸)(CH₂)_mC(O)OR⁸ (où m vaut de 0 à 3) ; -N(R⁸) (CH₂)_nC(O)OR⁸ (où n vaut de 1 à 3) ; -N((CH₂)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (où chaque n vaut de 1 à 3) ; -O(CH₂)_nC(O)N(R⁸)R⁹ (où n vaut de 1 à 3) ; -O(CH₂)_pC(O)OR⁸ (où p vaut de 1 à 6) ; -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (où chaque n vaut indépendamment de 1 à 3) ; un morpholin-4-yle, un 3-tétrahydrofuranoxy ;
ou R² est un aryloxy (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué de -OR⁸, de -C(O)N(R⁸)R⁹, d'un halogéno, d'un alkyle, d'un carboxy, d'un alcoxycarbonyle, d'un halogénalcoxy, d'un halogénoalcoxy-carbonyle, d'un alcoxycarbonylalkyle, d'un carboxyalkyle, d'un aminocarbonylalkyle, d'un (alkylamino) carbonylalkyle, d'un (dialkyl-amino)carbonylalkyle, d'un (arylamino) carbonyl-alkyle, d'un (aralkylamino) carbonylalkyle, d'un alcoxycarbonylalcényle, d'un carboxyalcényle, d'un aminocarbonylalcényle, d'un (alkylamino)-carbonylalcényle, d'un (dialkylamino)-carbonylalcényle, d'un (arylamino)-carbonylalcényle, d'un (aralkylamino)-carbonylalcényle, d'un (hydroxyalcoxy)-carbonyle, d'un (alcoxy)alcoxycarbonyle, d'un (hydroxyalcoxy)alcoxycarbonyle, d'un ((alcoxy)-alcoxy)alcoxycarbonyle, d'un tétrazolyle, d'un morpholin-4-ylalkyle et d'un (1,2)-imidazolinyle (éventuellement substitué par un alkyle)) ;
ou R² est un pipérazin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle) ;
ou R² est un 1-pipérazinoyle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxy, de -C(O)N(R⁸)R⁹, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);
ou R² est un (3,4)-pipéridinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkylcarbonyle, d'un carboxy, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle, d'un carboxyalkyle, d'un alcoxycarbonylalkyle et d'un tétrazolyl-alkyle) ;
ou R² est un pipéridin-4-ylamino (dans lequel l'amino est éventuellement substitué par un alkyle et le groupe pipéridinyle est éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un alcoxycarbonyle, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonylalkyle et d'un aralkyke) ;
ou R² est un 3-pyrrolidinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un alkyle, d'un aralkyle, d'un amidino, d'un 1-iminoéthyle, d'un carboxy, d'un carboxyalkyle, de -C(O)N(R⁸)R⁹, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle) ;

R⁴   est un hydrogène, -OR⁸ ou -N(R⁸)R⁹;

R⁵   est -C(NH)NH₂ ;

R⁶   est un guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -CH(OH)C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (où m vaut de 0 à 3), un 1-pipéridinoyle, un 1-pyrrolidinoyle, un (1,2)-imidazolyle (éventuellement substitué par un alkyle) ou un (1,2)-imidazolinyle (éventuellement substitué par un alkyle) ;

R⁷   est un hydrogène, un halogéno, un alkyle, -OR -C(O)N(R⁸)R⁹ ; .

R⁸ et R⁹   sont indépendamment un hydrogène, un méthyle, un éthyle ou un phényle ; et

R¹²   est un méthyle, un éthyle, un phényle ou un benzyle.

12. Composé selon la revendication 11, dans lequel

Z¹ et Z²   sont indépendamment -O- ou -NCH₃- ;

R¹ et R³   sont indépendamment un hydrogène, un fluoro, un chloro, un trifluorométhyle, un amino, -C(O)N(R⁸)R⁹ ou -NHC(O)NHR⁹ ;

R²   est un hydrogène ; un halogéno ; un alkyle ; un halogénoalcoxy ; -OR⁸ ; -C(O)OR⁸ ; -N(R⁸)R⁹ ; -N(R⁸)(CH₂)_nC(O)OR⁸ (où n vaut de 1 à 3) ; -N((CH2)_nN(R⁸)R⁹)(CH₂)_nC(O)OR⁸ (où chaque n vaut de 1 à 3) ; -O(CH2)_nC(O)N(R⁸)R⁹ (où n vaut de 1 à 3) ; -O(CH₂)_pC(O)OR⁸ (où p vaut de 1 à 6) ; -N(R⁸)(CH₂)_nC(O)N(R⁸)(CH₂)_nC(O)OR⁸ (où chaque n vaut indépendamment de 1 à 3) ; un morpholin-4-yle ; un 3-tétrahydrofuranoxy;
ou R² est un aryloxy (éventuellement substitué par un ou plusieurs substituants choisi indépendamment parmi le groupe constitué de -OR⁸, -C(O)N(R⁸)R⁹, d'un halogéno, d'un alkyle, d'un carboxy, d'un alcoxycarbonyle, d'un alcoxycarbonylalkyle, d'un carboxyalkyle, d'un alcoxycarbonylalcényle, d'un carboxyalcényle, d'un tétrazolyle, d'un morpholin-4-ylalkyle et d'un (1,2)-imidazolinyle (éventuellement substitué par un alkyle)) ;
ou R² est un pipérazin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis indépendamment parmi le groupe constitué d'un alkyle, d'un carboxyalkyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-1-yle (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxy et d'un alcoxycarbonyle) ;
ou R² est un (3,4)-pipéridinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxyalkyle et d'un alcoxycarbonylalkyle);
ou R² est un pipéridin-4-ylamino (où l'amino est éventuellement substitué par un alkyle et le groupe pipéridinyle est éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un carboxyalkyle, d'un alcoxycarbonylalkyle et d'un aralkyle) ;
ou R² est un 3-pyrrolidinyloxy (éventuellement substitué par un ou plusieurs substituants choisis parmi le groupe constitué d'un 1-iminoéthyle, d'un carboxy, d'un carboxyalkyle, d'un alcoxycarbonyle et d'un alcoxycarbonylalkyle);

R⁴   est un hydrogène, un amino, un hydroxy ou un méthoxy ;

R⁵   est -C(NH)NH₂ ;

R⁶   est un guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (où m vaut de 0 à 1), un (1,2)-imidazolyle substitué par un alkyle ou un 2-imidazolinyle substitué par un alkyle ;

R⁷   est un hydrogène, un méthoxy ou un hydroxy ; et

R⁸ et R⁹   sont indépendamment un hydrogène, un méthyle, un éthyle ou un phényle.

13. Composé selon la revendication 12, dans lequel

Z¹ et Z²   sont tous les deux -O- ;

R¹   sont indépendamment un hydrogène, un fluoro ou un chloro ;

R⁴   est un hydrogène, un amino, un hydroxy ou un méthoxy ;

R⁶   est un guanidino, -C(NH)NH₂, -C(O)N(R⁸)R⁹, -(CH₂)_mN(R⁸)R⁹ (où m vaut 0 ou 1), un (1,2)-imidazolyle substitué par un méthyle ou un 2-imidazolinyle éventuellement substitué par un méthyle ; et

R⁷   est un hydrogène ou un hydroxy.

14. Composé selon la revendication 13, dans lequel

R⁴   est un hydroxy ;

R⁶   est un diméthylamino ou un diméthylamino-carbonyle ; et

R⁷   est un hydrogène.

15. Composé selon la revendication 14, choisi parmi le groupe constitué des composés suivants :

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-2-méthoxypyridin-4-yl)oxy]-benzamidine et

la 4-hydroxy-3-[(3,5-difluoro-6-(3-diméthylaminocarbonylphénoxy)-2-(2-méthoxy-5-éthoxycarbonylphénoxy)pyridin-4-yl)oxy]benzamidine.

16. Composition pharmaceutique utile pour le traitement d'un être humain atteint d'un état maladif caractérisé par une activité thrombotique, laquelle composition comprend une quantité thérapeutiquement efficace d'un composé selon l'une quelconque des revendications précédentes.

17. Utilisation d'une quantité thérapeutiquement efficace d'un composé selon les revendications 1 à 15 pour la fabrication d'un médicament destiné au traitement d'un état maladif caractérisé par une activité thrombotique.

18. Composé selon l'une quelconque des revendications 1 à 15, destiné à être utilisé en tant que médicament.

19. Utilisation selon la revendication 17, dans laquelle le médicament est un anticoagulant.

20. Utilisation selon les revendications 17 ou 19, dans laquelle le traitement met en jeu une prophylaxie pour un risque à long terme à la suite d'un infarctus du myocarde, une prophylaxie de la thrombose veineuse profonde (TVP) à la suite d'une chirurgie orthopédique, une prophylaxie de patients sélectionnés à la suite d'une attaque ischémique transitoire ; un traitement de la thrombose veineuse profonde (TVP) ; un traitement associé à une intervention chirurgicale telle qu'un pontage artério-coronarien par greffe et l'angioplastie coronarienne transluminale percutanée ; un traitement de complications thrombotiques associés à une leucémie promyélocytique aiguë, du diabète, de myélomes multiples, d'une coagulation intravasculaire disséminée associée à un choc septique, d'une infection associée à purpura fulminanas, du syndrome de détresse respiratoire chez l'adulte, de l'angine instable, et de complications thrombotiques associées à une prothèse de valve aortique ou vasculaire ; une prophylaxie pour des maladies thrombotiques, en particulier chez des patients à haut risque de développer une telle maladie.