首页> 外国专利> NEW DERIVATIVES OF 6-AMINO-7-HYDROXY-4,5,6,7-TETRAHYDROIMIDAZO(4,5,L-J-K)(1)-BENZAZEPIN-2(1H)-ONE,THEIR SALTS,THEIR PREPARATION,THEIR APPLICATION AS MEDICAMENTS,AND THE COMPOSITIONS CONTAINING THEM

NEW DERIVATIVES OF 6-AMINO-7-HYDROXY-4,5,6,7-TETRAHYDROIMIDAZO(4,5,L-J-K)(1)-BENZAZEPIN-2(1H)-ONE,THEIR SALTS,THEIR PREPARATION,THEIR APPLICATION AS MEDICAMENTS,AND THE COMPOSITIONS CONTAINING THEM

机译:6-氨基-7-羟基-4,5,6,7-四氢咪达唑(4,5,LJK)(1)-苯并ZE庚因-2(1H)-的新衍生物,其盐,其制备方法,其在药物中的应用,以及包含它们的组成

摘要

Novel 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,l-j-k][1]-benzazepin- 2-(1H)-one derivatives of the formula IMAGE wherein R is selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms optionally substituted with a hydroxyl, aryl and aryloxy of 6 to 10 carbon atoms, cycloalkyl of 3 to 7 carbon atoms optionally interrupted with a heteroatom optionally substituted with alkyl of 1 to 4 carbon atoms and the wavy lines indicates that the 7-OH and 6-amino have the trans configuration and their non-toxic, pharmaceutically acceptable acid addition salts having remarkable anti-hypertensive and hypotensive activity and vasodilatatory activity and their preparation.
机译:的新型6-氨基-7-羟基-4,5,6,7-四氢咪唑并[4,5,1k] [1]-苯并ze庚因-2-(1H)-一衍生物,其中R为选自氢,1至8个碳原子的烷基,任选被6至10个碳原子的羟基,芳基和芳氧基取代,3至7个碳原子的环烷基,任选被1至1个烷基取代的杂原子中断4个碳原子和波浪线表示7-OH和6-氨基具有反式构型,并且其无毒的药学上可接受的酸加成盐具有显着的抗高血压和降血压活性以及血管舒张活性及其制备方法。

著录项

  • 公开/公告号IL69993D0

    专利类型

  • 公开/公告日1984-01-31

    原文格式PDF

  • 申请/专利权人 ROUSSEL UCLAF;

    申请/专利号IL19830069993

  • 发明设计人

    申请日1983-10-18

  • 分类号C07D;

  • 国家 IL

  • 入库时间 2022-08-22 09:17:16

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