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Method for preparing chromone- and thiochromone-substituted 1,4-dihydropyridine derivatives

机译:色酮和硫代色酮取代的1,4-二氢吡啶衍生物的制备方法

摘要

Dihydropyridines of the formula IMAGE in which R1, R2, R5, R6, R7 and R8 can be hydrogen or various halogen or organic radicals, R4 is an optionally substituted hydrocarbon radical, A is a direct bond, an alkylene chain with 1 to 20 C atoms or an alkenylene chain with 2 to 20 atoms, the chains being optionally interrupted by O or S, X is O or S and Y is a direct bond, O, S, -NH- or -N- alkyl with 1 to 8 C atoms, or a pharmaceutically acceptable salt thereof, are useful as cardiotonic agents for improving heart contractility, antihypotonic agents, for lowering the blood sugar level, for detumescing mucous membranes and for influencing the salt and liquid balance.
机译:的二氢吡啶,其中R 1,R 2,R 5,R 6,R 7和R 8可以是氢或各种卤素或有机基团,R 4是任选取代的烃基,A是直接键,具有1至1的亚烷基链。 20个C原子或2至20个原子的亚烯基链,该链可选地被O或S中断,X为O或S,且Y为直接键,O,S,-NH-或-N-烷基具有1至8 C原子或其药学上可接受的盐可用作用于改善心脏收缩力的强心剂,抗低渗剂,降低血糖水平,使粘膜消肿以及影响盐和液体平衡。

著录项

  • 公开/公告号KR840008023A

    专利类型

  • 公开/公告日1984-12-12

    原文格式PDF

  • 申请/专利权人 귄터 페터스;

    申请/专利号KR19840001522

  • 发明设计人 지그프리트 골드만 (외 4);

    申请日1984-03-24

  • 分类号C07D405/04;

  • 国家 KR

  • 入库时间 2022-08-22 08:01:13

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