首页> 外国专利> N-(BENZAZEPIN-3-YL)-AND N-(BENZODIAZEPIN-3-YL)-ALKYLENE-N-INDOL-3-YL-ALKYLENE-AMINE DERIVATIVES,THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

N-(BENZAZEPIN-3-YL)-AND N-(BENZODIAZEPIN-3-YL)-ALKYLENE-N-INDOL-3-YL-ALKYLENE-AMINE DERIVATIVES,THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

机译:N-(苯并二氮杂-3-基)-和N-(苯并二氮杂-3-基)-亚烷基-N-吲哚-3-基-亚烷基-胺基衍生物,它们的制备和药物成分

摘要

This invention relates to novel indole derivatives of the formula IMAGE (I) wherein A represents a -CH2-CH2-, -CH=CH-, IMAGE group and B represents a methylene, carbonyl, or thiocarbonyl group or A represents a -CO-CO- or IMAGE group and B represents a methylene group, E represents an alkylene group or a 2-hydroxy-n-propylene, 2-hydroxy-n-butylene, or 3-hydroxy-n-butylene group, G represents an alkylene group, R1 represents a hydrogen, chlorine, or bromine atom or a trifluoromethyl, nitro, amino, alkylamino, dialkylamino, alkyl, hydroxyl, alkoxy, or phenylalkoxy group, R2 represents a hydrogen, chlorine, or bromine atom or a hydroxyl, alkoxy, phenylalkoxy, or alkyl group or R1 and R2 together represent an alkylenedioxy group, R3 represents a hydrogen, chlorine, or bromine atom or an alkyl group, R4 represents a hydrogen atom or an alkyl or phenylalkyl group, R5 represents a hydrogen, fluorine, chlorine, or bromine atom or an alkyl, hydroxyl, alkoxy, or phenylalkoxy group, R6 represents a hydrogen atom or an alkoxy group, and R7 represents a hydrogen atom or an alkenyl, alkyl or phenylalkyl group, and the acid additional salts thereof. These compounds, which may be obtained by use of known methods, have valuable pharmacological properties, particularly a heart rate-lowering activity.
机译:本发明涉及式(I)的新型吲哚衍生物,其中A代表-CH 2 -CH 2-,-CH = CH-,基团,B代表亚甲基,羰基或硫代羰基,或A代表-CO-CO-或基团,B代表亚甲基,E代表亚烷基或2-羟基-正丙烯基,2-羟基-正丁烯基或3-羟基-正丁烯基,G代表亚烷基,R1代表氢,氯或溴原子或三氟甲基,硝基,氨基,烷基氨基,二烷基氨基,烷基,羟基,烷氧基或苯基烷氧基,R2代表氢,氯或溴原子或羟基,烷氧基,苯基烷氧基或烷基,或R 1和R 2一起代表亚烷基二氧基,R 3代表氢,氯或溴原子或烷基,R 4代表氢原子或烷基或苯基烷基,R 5代表氢,氟,氯或溴原子或烷基,羟基,烷氧基或苯基烷氧基, R 6代表氢原子或烷氧基,R 7代表氢原子或烯基,烷基或苯基烷基,及其酸的另外的盐。可以通过使用已知方法获得的这些化合物具有有价值的药理特性,特别是降低心率的活性。

著录项

  • 公开/公告号IL73696A

    专利类型

  • 公开/公告日1987-10-30

    原文格式PDF

  • 申请/专利权人 DR. KARL THOMAE GMBH;

    申请/专利号IL19840073696

  • 发明设计人

    申请日1984-11-30

  • 分类号C07D403/12;C07D491/02;A61K31/55;

  • 国家 IL

  • 入库时间 2022-08-22 07:20:14

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