首页> 外国专利> Process for preparing 9- (monosubstituted propoxymethyl 1-0 or 3-0 or disubstituted in 1.3 to 0) from 1.3 to 0 -purinas substituted) are substituted as agents -purinas them antivira-

Process for preparing 9- (monosubstituted propoxymethyl 1-0 or 3-0 or disubstituted in 1.3 to 0) from 1.3 to 0 -purinas substituted) are substituted as agents -purinas them antivira-

机译:从1.3到0制备9-(单取代的丙氧基甲基1-0或3-0或在1.3到0中被二取代)-取代的嘌呤被取代为试剂-嘌呤被抗病毒-

摘要

Compounds useful as antiviral agents are defined by the following formula: IMAGE (I) wherein R1 is hydrogen, -C(Y)OR7 or -C(O)NHR7 wherein R7 is alkyl of one to twelve carbon atoms, alkenyl of two to twelve carbon atoms, cyclopentyl, cyclohexyl, phenyl or benzyl; R2 is -C(Y)OR7 or -C(O)NHR7 wherein R7 is as defined above; Y is oxygen or sulfur; R3 is hydrogen, halo, thio, lower alkylthio of one to six carbon atoms, azido, NR9R10 wherein R9 and R10 are independently hydrogen or lower alkyl of one to six carbon atoms or -NHC(O)R8 wherein R8 is hydrogen, alkyl of one to nineteen carbon atoms or 1-adamantyl; and (a) R6 is hydrogen, halo, lower alkoxy of one to six carbon atoms, azido, thio, lower alkylthio of one to six carbon atoms, -NR9R10 wherein R9 and R10 are as defined above or -NHC(O)R8 wherein R8 is as defined above and R4 together with R5 is a bond; or (b) R5 together with R6 is a keto group and R4 is hydrogen.
机译:用作抗病毒剂的化合物由下式定义:(I)其中R1为氢,-C(Y)OR7或-C(O)NHR7其中R7为具有十二至十二个碳原子的烷基,两个烯基至十二个碳原子,环戊基,环己基,苯基或苄基; R2是-C(Y)OR7或-C(O)NHR7,其中R7如上所定义; Y是氧或硫; R3是氢,卤素,硫代,1-6个碳原子的低级烷硫基,叠氮基,NR9R10(其中R9和R10独立地是氢或1-6个碳原子的低级烷基)或-NHC(O)R8其中R8是氢, 1至19个碳原子或1-金刚烷基; (a)R6是氢,卤素,1-6个碳原子的低级烷氧基,叠氮基,硫代,1-6个碳原子的低级烷硫基,-NR9R10,其中R9和R10如上定义或-NHC(O)R8,其中R8如上定义,并且R4与R5一起是键; (b)R5与R6一起是酮基,R4是氢。

著录项

  • 公开/公告号ES545261A0

    专利类型

  • 公开/公告日1986-01-01

    原文格式PDF

  • 申请/专利权人 SYNTEX (U.S.A.) INC.;

    申请/专利号ES19850545261

  • 发明设计人

    申请日1985-07-16

  • 分类号C07D473/00;A61K31/52;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:50

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