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Process for preparing derivatives aminoisoquinolinosasi and their acid addition salts, pharmaceutically acceptable and their quaternary ammonium derivatives

机译:氨基异喹啉基衍生物及其酸加成盐,药学上可接受的及其季铵衍生物的制备方法

摘要

Novel aminoisoquinoline derivatives of the general formula (I) IMAGE (I) wherein R1 represents a hydrogen atom or a C1-4 alkyl group, R2 represents a hydrogen atom, R3 represents a hydrogen atom, R4 represents a morpholinyl group or a piperazinyl group substituted with a pyridyl group, and pharmaceutically acceptable acid addition salts and quaternary derivatives thereof have been prepared. The novel compounds exert narcosis potentiating effects.
机译:通式(I)(I)的新型氨基异喹啉衍生物,其中R1代表氢原子或C1-4烷基,R2代表氢原子,R3代表氢原子,R4代表吗啉基或哌嗪基已经制备了被吡啶基取代的基团,及其药学上可接受的酸加成盐和季衍生物。新型化合物具有增强麻醉作用。

著录项

  • 公开/公告号ES490506A0

    专利类型

  • 公开/公告日1981-02-16

    原文格式PDF

  • 申请/专利权人 EGYT GYOGYSZERVEGYESZETI GYAR;

    申请/专利号ES19800490506

  • 发明设计人

    申请日1980-04-11

  • 分类号C07D215/38;A61K31/47;

  • 国家 ES

  • 入库时间 2022-08-22 15:51:07

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