(19)
(11)EP 0 355 986 A1

(12)EUROPEAN PATENT APPLICATION

(43)Date of publication:
28.02.1990 Bulletin 1990/09

(21)Application number: 89307268.6

(22)Date of filing:  18.07.1989
(51)International Patent Classification (IPC)5C07D 473/32
(84)Designated Contracting States:
BE CH DE ES FR GB IT LI NL

(30)Priority: 20.07.1988 GB 8817270

(71)Applicant: BEECHAM GROUP plc
Brentford, Middlesex TW8 9EP (GB)

(72)Inventor:
  • Kincey, Peter Markham
    The Pinnacles, HARLOW, Essex CM19 5AD (GB)

(74)Representative: Tocher, Pauline et al
SmithKline Beecham plc Corporate Intellectual Property SB House Great West Road
Brentford, Middlesex TW8 9BD
Brentford, Middlesex TW8 9BD (GB)


(56)References cited: : 
  
     
    Remarks:
    The title of the invention has been amended (Guidelines for Examination in the EPO, A-III, 7.3).
     


    (54)2-Aminopurine preparation process


    (57) A process for the preparation of a compound of formula (I):

    which process comprises the reduction of a compound of formula (II):

    by catalytic hydrogenation using palladium on charcoal as catalyst.


    Description


    [0001] The present invention relates to a process for the preparation of a compound which is useful as an intermediate in the preparation of compounds which are antiviral agents.

    [0002] The compound 2-aminopurine of formula (I):

    is a potentially useful intermediate in the preparation of 6-deoxy guanine nucleoside analogues, for example as described in EP-A-108285 (The Wellcome Foundation Limited), EP-A-182024 (Beecham Group p.l.c.) and EP-A-186640 (Astra Läkemedal Aktiebolag).

    [0003] A suitable method of preparation involves the condensation of a side chain intermediate RQ wherein R is a side chain residue or a moiety convertible thereto, and Q is a leaving group, with the compound of formula (I), wherein the amino group is optionally protected, followed by subsequent conversion of R and deprotection, if necessary to give a compound of formula (A):



    [0004] Compounds of formula (A) which are antiviral agents include the following:
    CompoundR
    6-Deoxyacyclovir -(CH₂)₄OH
    6-Deoxy DHPG -OCH₂CH(CH₂OH)₂
    6-Deoxy DHBG -(CH₂)₂CH(OH)CH₂OH
    BRL 42810 -(CH₂)₂CH(CH₂OAc)₂


    [0005] Present preferred methods for obtaining compounds of formula (A) involve condensation of RQ with alternative compounds to 2-aminopurine, such as guanine itself or 2-amino-6-chloropurine, followed by an additional conversion step of 6-OH/6-Cl to 6-hydrogen. This is because 2-aminopurine itself is relatively expensive and not easily obtainable commercially, and a reliable, or high yielding method synthesis has not been available.

    [0006] Kusmierek et al. (Acta Chem. Scand., Ser. B41: 701-707) have described a method of preparation of 2-aminopurine from 2-amino-6-chloropurine by electrolytic reduction.

    [0007] We have now discovered an improved method which has the advantages of simplicity and hence is less expensive, and has greater potential for large scale production.

    [0008] Accordingly, the present invention provides a process for the preparation of a compound of formula (I):

    which process comprises the reduction of a compound of formula (II):

    by catalytic hydrogenation using palladium on charcoal as catalyst.

    [0009] The reaction usually takes place in an aqueous solution preferably in the presence of a base, such as sodium hydroxide, at a temperature of 5oC to 100oC, preferably around 50oC.

    [0010] The hydrogenation takes place at a pressure of 15 psi to 1500 psi (10.5 to 1050 kPa), preferably 100 psi (5200 mm Hg or 700 kPa), for a period of 75 min. to 24 hours, preferably about 3 hours.

    [0011] The product is extracted by conventional methods, such as those described in the Example hereinafter.

    [0012] The following Example illustrates the invention. The following Preparation Example describes the use of the compound of formula (I) in the preparation of BRL 42810.

    Example


    2-Aminopurine



    [0013] 



    [0014] 2-Amino-6-chloropurine (84.8g, 0.5mol) was dissolved in a solution of sodium hydroxide (50.0g, 1.25mol) in water (500ml). The resulting solution was added to 5% palladium on charcoal (10.0g) and hydrogenated at 100 psi and 50oC for 3 hours. The catalyst was filtered off, the filtrate was acidified to pH 8.0 with 2M hydrochloric acid, and the solution filtered to remove solid impurities. The filtrate was then further acidified to pH 5.5 and allowed to stand at 4oC overnight. The precipitated product was filtered off, washed with ice-cold water, then acetone, and dried in vacuo at 50oC.
    Yield 56.6, (83%) m.p. 277oC
    ¹H nmr (d₆-DMSO) δ6.35(br s,2H,NH₂), 8.13(s,1H,H8), 8.65(s,1H,H6).

    Preparation Example


    BRL 42810 from 2-aminopurine



    [0015] 



    [0016] A mixture of 2-aminopurine (3.4g, 0.025mol), 2-acetoxymethyl-4-iodo-butyl-1-acetate (7.9g, 0.025mol), anhydrous potassium carbonate (5.2g, m0.0375 mol) and dry dimethylformamide (50 ml) was stirred under nitrogen at room temperature for 18 hours. The mixture was filtered through celite, and the filter bed washed with dimethylformamide (50ml), the combined filtrates were evaporated to an oil, which was purified by column chromatography on silica gel (150g), eluting with 95% chloroform/5% methanol, to give BRL 42810 as a white solid.
    Yield 4.7g (58%) m.p. 102oC
    ¹H nmr (d₆-DMSO) δ1.88(m,3H), 2.00(s,6H, 4.03(d,4H), 4.14(t,2H), 6.45(br s,2H), 8.09(s,1H), 8.57(s,1H).


    Claims

    1. A process for the preparation of a compound of formula (I):

    which process comprises the reduction of a compound of formula (II):

    by catalytic hydrogenation using palladium on charcoal as catalyst.
     
    2. A process according to claim 1 wherein the reduction reaction takes place in aqueous solution in the presence of a base.
     
    3. A process according to claim 2 wherein the base is sodium hydroxide.
     
    4. A process according to any one of claims 1 to 3 wherein the reaction is carried out at a temperature of around 50oC.
     
    5. A process according to any one of claims 1 to 4 wherein the hydrogenation takes place at a pressure of around 70 kPa.
     
    6. A process for the preparation of a compound of formula (I) as defined in claim 1 essentially as herein described with reference to the Example.
     
    7. A compound of formula (I) as defined in claim 1 whenever prepared by the process according to any one of claims 1 to 6.
     
    8. Use of a compound according to claim 7 in the preparation of 6-deoxy guanine nucleoside analogue antiviral agent.
     
    9. A use according to claim 8 wherein the 6-deoxy guanine nucleoside analogue antiviral agent is BRL 42810.
     





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