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Process for preparing derivatives quanadina.

机译:制备衍生物夸纳迪纳的方法。

摘要

The invention relates to guanidine derivatives which are histamine H-2 antagonists and which inhibit gastric acid secretion. According to the invention there is provided a guanidine derivative of the formula I:- IMAGE I in which R1 and R2, same or different, are hydrogen or 1-10C alkyl, 3-8C cycloalkyl or 4-14C cycloalkylalkyl, each alkyl, cycloalkyl or cycloalkylalkyl optionally carrying one or more F, Cl or Br atoms, provided that one of R1 and R2 is halogen substituted, or R2 is hydrogen and R1 is R5-E-W in which W is 2-6C alkylene optionally substituted by 1 or 2 1-4C alkyls, E is O,S or NR6 in which R6 is H or 1-6C alkyl, R5 is H or 1-6C alkyl optionally substituted by 1 or 2 1-4C alkyls, or R5 and R6 are joined to form a pyrrolidine, piperidine, morpholine, piperazine or N-methylpiperazine ring; ring X is a heterocyclic ring as defined in the specification; A is phenylene or 5-7C cycloalkylene, or a 1-8C alkylene into which is optionally inserted one or two groups; D is O or S; and R3 and R4 are hydrogen or a variety of radicals described in the specification: and the pharmaceutically-acceptable acid-addition salts thereof. Manufacturing processes and pharmaceutical compositions are also described.
机译:本发明涉及作为组胺H-2拮抗剂并抑制胃酸分泌的胍衍生物。根据本发明,提供式I的胍衍生物:其中R 1和R 2相同或不同,为氢或1-10C烷基,3-8C环烷基或4-14C环烷基烷基,每个烷基,任选地带有一个或多个F,Cl或Br原子的环烷基或环烷基烷基,条件是R1和R2中的一个被卤素取代,或R2是氢且R1是R5-EW,其中W是2-6C的亚烷基,可选地被1或3取代2 1-4C烷基,E为O,S或NR6,其中R6为H或1-6C烷基,R5为任选被1或2个1-4C烷基取代的H或1-6C烷基,或将R5和R6连接至形成吡咯烷,哌啶,吗啉,哌嗪或N-甲基哌嗪环;环X是如说明书中所定义的杂环; A为亚苯基或5-7C亚环烷基,或任选插入一个或两个基团的1-8C亚烷基; D是O或S; R3和R4是氢或说明书中描述的各种基团:及其药学上可接受的酸加成盐。还描述了制造过程和药物组合物。

著录项

  • 公开/公告号ES510258A0

    专利类型

  • 公开/公告日1983-04-16

    原文格式PDF

  • 申请/专利权人 ICI PLC;ICI AMERICA INC;

    申请/专利号ES19820510258

  • 发明设计人

    申请日1982-03-09

  • 分类号C07C133/10;A61K31/155;

  • 国家 ES

  • 入库时间 2022-08-22 10:47:35

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