Global Patent Index - EP 2262814 A1

EP 2262814 A1 20101222 - 4'4'-DIOXASPIRO-SPIROCYCLICALLY SUBSTITUTED TETRAMATES

Title (en)

4'4'-DIOXASPIRO-SPIROCYCLICALLY SUBSTITUTED TETRAMATES

Title (de)

4'4'-DIOXASPIRO-SPIROCYCLISCH SUBSTITUIERTE TETRAMATE

Title (fr)

TÉTRAMATES SPIROCYCLIQUES À SUBSTITUTION 4'4'-DIOXASPIRO

Publication

EP 2262814 A1 20101222 (DE)

Application

EP 09721839 A 20090316

Priority

  • EP 2009001897 W 20090316
  • EP 08153002 A 20080319
  • EP 09721839 A 20090316

Abstract (en)

[origin: EP2103615A1] 4'4'-Dioxaspiro-spirocyclically substituted terminates (I), are new. 4'4'-Dioxaspiro-spirocyclically substituted terminates of formula (I), are new. W 1>H, alkyl, alkenyl, alkynyl, halo, alkoxy, haloalkyl, haloalkoxy or CN; X : halo, alkyl, alkenyl, alkynyl, alkoxy, haloalkyl, haloalkoxy, NO 2or CN; Y 1>, Z : H, alkyl, alkenyl, alkynyl, alkoxy, halo, haloalkyl, haloalkoxy, CN or NO 2; AB 1>C : 5-6-membered ketal (optionally substituted by alkyl, haloalkyl, alkoxy, alkoxyalkyl or optionally substituted phenyl); G : metal ion equivalent or ammonium ion; and m, n : 1-2. Independent claims are included for: (1) the preparation of (I); (2) an agent comprising an active agent combination comprising (I), and at least a compound for improving the crop plant compatibility such as: e.g. AD-67, MON-4660, dicyclonone (BAS-145138), benoxacor, 5-chloro-quinolin-8-oxy-acetic acid-(1-methyl-hexylester), cumyluron, cyometrinil, 2,4-D, 2,4-DB, daimuron, dymron, dicamba, dimepiperate, DKA-24, dichlormid, fenclorim, flurazole, fluxofenim, furilazole (MON-13900), lactidichlor, 4-chloro-o-(tolyloxy)-acetic acid, mecoprop, 2-dichloromethyl-2-methyl-1,3-dioxolane, 2-propenyl-1-oxa-4-azaspiro[4.5]decane-4-carbodithioate, 1,8-naphthalic acid anhydride, oxabetrinil, 2,2-dichloro-N-(1,3-dioxolan-2-yl-methyl)-N-(2-propenyl)-acetamide, 3-dichloroacetyl-2,2-dimethyl-oxazolidine, 3-dichloroacetyl-2,2,5-trimethyloxazolidine, 4-(4-chloro-o-tolyl)-butteric acid, 4-(4-chloro-phenoxy)-butteric acid, diphenylmethoxy acetic acid, diphenylmethoxy acetic acid-methylester, diphenylmethoxy acetic acid-ethylester, 1-(2-chloro-phenyl)-5-phenyl-1H-pyrazol-3-carboxylic acid-methylester, 1,2-(dichloro-phenyl)-5-methyl-1H-pyrazol-3-carboxylic acid-ethylester, 1-(2,4-dichlorophenyl)-5-isopropyl-1H-pyrazol-3-carboxylic acid-ethylester, 1-(2,4-dichloro-phenyl)-5-(1,1-dimethyl-ethyl)-1H-pyrazol-3-carboxylic acid-ethylester, 5-(2,4-dichloro-benzyl)-2-isoxazolin-3-carboxylic acid-ethylester, 5-phenyl-2-isoxazolin-3-carboxylic acid-ethylester, 5-chloro-quinolin-8-oxy-acetic acid-4-allyloxy-butylester, 5-chloro-quinolin-8-oxy-acetic acid-1-allyloxy-prop-2-yl-ester, 5-chloroquinioxalin-8-oxy-acetic acid-methylester, 5-chloro-quinolin-8-oxy-acetic acid-ethylester, 5-chloro-quinoxalin-8-oxy-acetic acid-allylester, 4-chloro-phenoxy-acetic acid, 1-[4-(N-2-methoxybenzoylsulfamoyl)-phenyl]-3,3-dimethyl-urea, 1-[4-(N-4, 5-dimethylbenzoylsulfamoyl)-phenyl]-3-methyl-urea, 1-[4-(N-naphthylsulfamoyl)-phenyl]-3,3-dimethyl-urea and/or N-(2-methoxy-5-methylbenzoyl)-4-(cyclopropylaminocarbonyl)-benzene sulfonamide, preferably cloquintocet-mexyl, fenchlorazole-ethyl, isoxadifen-ethyl, mefenpyr-diethyl, furilazole, fenclorim, cumyluron, dymron, or N-cyclopropyl-4-(2-methoxy-5-methyl-benzoylsulfamoyl)-benzamide or N-cyclopropyl-4-(2-methoxy-benzoylsulfamoyl)-benzamide; (3) a first composition comprising a substituted 4-hydroxy-3-phenyl-1-aza-spiro[4.5]dec-3-en-2-one compound of formula (IIa), (I) and at least a solvent; (4) a second composition comprising (I) and at least a salt of formula ([D1 +>(R26a)(R27a)(R28a)(R29a)] n(R30a (n ->))) (IIb); (5) preparing the agent, comprising mixing the first composition with stretching agent and/or surface active materials; and (6) preparing the first composition, comprising adding the components of the composition of a water mixable solvent or water. D1 : N or P; R26a-R29a : 1-8C-alkyl, 1 or more times unsaturated 1-8C-alkylene (both optionally substituted by halo, NO 2or CN), or H; R30a : an inorganic or organic anion; and n : 1-4. [Image] [Image] ACTIVITY : Pesticide; Herbicide; Acaricide; Insecticide; Anthelmintic; Nematocide; Arthropodicide; Antiparasitic; Fungicide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.

IPC 8 full level

C07D 491/113 (2006.01); A01N 43/90 (2006.01)

CPC (source: EP US)

A01N 43/90 (2013.01 - EP US); C07D 491/113 (2013.01 - EP US)

Citation (search report)

See references of WO 2009115262A1

Designated contracting state (EPC)

AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR

Designated extension state (EPC)

AL BA RS

DOCDB simple family (publication)

EP 2103615 A1 20090923; AR 070909 A1 20100512; AU 2009226704 A1 20090924; BR PI0910229 A2 20150901; BR PI0910229 B1 20180214; CA 2718735 A1 20090924; CL 2009000555 A1 20100305; CN 101977916 A 20110216; CO 6382165 A2 20120215; EP 2262814 A1 20101222; JP 2011515352 A 20110519; KR 20100126516 A 20101201; MX 2010009295 A 20100924; TW 201000012 A 20100101; US 2011086762 A1 20110414; WO 2009115262 A1 20090924; ZA 201006127 B 20111026

DOCDB simple family (application)

EP 08153002 A 20080319; AR P090100935 A 20090316; AU 2009226704 A 20090316; BR PI0910229 A 20090316; CA 2718735 A 20090316; CL 2009000555 A 20090309; CN 200980109827 A 20090316; CO 10102872 A 20100820; EP 09721839 A 20090316; EP 2009001897 W 20090316; JP 2011500094 A 20090316; KR 20107023109 A 20090316; MX 2010009295 A 20090316; TW 98108691 A 20090318; US 93304009 A 20090316; ZA 201006127 A 20100827