首页> 外国专利> PYRIMIDO(6,1-A)ISOQUINOLIN-4-ONE AND PYRIMIDO(6,1-A)-BENZAZEPIN-4-ONE DERIVATIVES,THEIR MANUFACTURE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

PYRIMIDO(6,1-A)ISOQUINOLIN-4-ONE AND PYRIMIDO(6,1-A)-BENZAZEPIN-4-ONE DERIVATIVES,THEIR MANUFACTURE AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

机译:PYRIMIDO(6,1-A)异喹诺酮-4-酮和PYRIMIDO(6,1-A)-苯并ZE杂-4-酮衍生物,其制备和组成它们的药物组合物

摘要

RAN 4044/62AbstractPyrimidone derivatives of the formula Iwherein n is the number 1 or 0,X, A1 and A2 are optionally mono-lower alkylatedor di-lower alkylated methylene,or X is optionally lower alkylated nitrogen,R is hydrogen or lower-alkyl and Y andZ together are a group =NR5,or R and Z together are a N-C-bond and Yis a group -N(H)R5,R1, R2 and R3 are hydrogen, lower-alkyl orlower-alkoxy,or two of R1, R2 and R3 on adjacent carbonatoms are methylenedioxy or ethylenedioxy,R4 is hydrogen or lower-alkyl,R5 is phenyl optionally substituted by R6,R7 and R8,and R6, R7 and R8 are chlorine, fluorine,bromine, lower-alkyl or lower-alkoxy,with the proviso that at least one of themethylene groups A1 and A2 is mono-lower alkylatedox di-lower alkylated when R4 is hydrogen and nis the number 0,and physiologically compatible salts thereof have bloodplatelet aggregation-inhibiting activity or have activityon the circulatory system.These compounds are obtained starting from corres-ponding chlorinated or brominated pyrimidone derivatives.
机译:RAN 4044/62抽象式的嘧啶酮衍生物 一世其中n是数字1或0,X,A1和A2可选为单低级烷基化或二低级烷基化的亚甲基,或X是任选的低级烷基化氮,R为氢或低级烷基,且Y为Z一起是一个组= NR5,或R和Z一起是N-C键和Y是-N(H)R5组,R1,R2和R3为氢,低级烷基或低级烷氧基或相邻碳原子上的R1,R2和R3中的两个原子是亚甲二氧基或亚乙二氧基,R4是氢或低级烷基,R5是任选被R6取代的苯基,R7和R8,R6,R7和R8是氯,氟溴,低级烷基或低级烷氧基,附带条件是,至少亚甲基A1和A2是单低级烷基化的当R4为氢和n时,ox di-lower烷基化是数字0,及其生理相容性盐有血血小板聚集抑制活性或具有活性在循环系统上。这些化合物是从正确的方法获得的-思考氯化或溴化嘧啶酮衍生物。

著录项

  • 公开/公告号IL71711A

    专利类型

  • 公开/公告日1987-08-31

    原文格式PDF

  • 申请/专利权人 F. HOFFMANN - LA ROCHE & CO.AKTIENGESELLSCHAFT;

    申请/专利号IL19840071711

  • 发明设计人

    申请日1984-05-01

  • 分类号C07D487/04;A61K31/505;C07D471/04;

  • 国家 IL

  • 入库时间 2022-08-22 07:20:15

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