Thioformamide derivative, process for its preparation, pharmaceutical
composition thereof and treatment method
    3.
    发明授权
    Thioformamide derivative, process for its preparation, pharmaceutical composition thereof and treatment method 失效
    硫代甲酰胺衍生物,其制备方法,药物组合物和治疗方法

    公开(公告)号:US5276045A

    公开(公告)日:1994-01-04

    申请号:US860599

    申请日:1992-03-30

    摘要: A thioformamide derivative of the formula: ##STR1## wherein R represents alkyl, A represents optionally substituted pyrid-3-yl, isoquinolin-4-yl, tetrahydroquinolin-3-yl, quinolin-3-yl, pyridazin-4-yl, pyrimid-5-yl, thiazol-5-yl, thieno[2,3-b]pyridin-5-yl, pyrazin-2-yl, indol-3-yl and thieno[3,2-b]pyridin-6-yl, or phenyl and Y represents a valency bond, methylene or ethylene, R.sup.2 represents hydrogen, optionally substituted alkyl, cycloalkyl, cycloalkylalkyl, aryl, aralkyl, aryloxyalkyl, aromatic heterocyclylalkyl or aromatic heterocyclyloxyalkyl group or a group ZC(.dbd.O)-- in which Z represents optionally substituted alkyl, aryl, or aromatic heterocyclic, n represents 0 or 1, and when n represents 0, R.sup.1 may represent a hydrogen atom, optionally substituted alkyl, cycloalkyl, cycloalkylalkyl, aryl, aralkyl, aryloxyalkyl, aromatic heterocyclylalkyl or aromatic heterocyclyloxyalkyl group or a group ZC(.dbd.O)-- or ZSO.sub.2 --, and when n represents 1, R.sup.1 represents optionally substituted alkyl, benzyl, phenethyl, 1-naphthylmethyl, 2-naphthylmethyl or pyrid-3-ylmethyl radical and pharmaceutically acceptable salts thereof possess pharmacological properties.

    摘要翻译: 下式的硫代甲酰胺衍生物其中R代表烷基,A代表任意取代的吡啶-3-基,异喹啉-4-基,四氢喹啉-3-基,喹啉-3-基,哒嗪-4-基, 嘧啶-5-基,噻唑-5-基,噻吩并[2,3-b]吡啶-5-基,吡嗪-2-基,吲哚-3-基和噻吩并[3,2-b] 芳基,芳烷基,芳氧基烷基,芳族杂环基烷基或芳族杂环基氧基烷基或基团ZC(= O) - ,其中R 1表示氢,烷基,环烷基,环烷基烷基,芳基, Z表示任选取代的烷基,芳基或芳族杂环,n表示0或1,当n表示0时,R 1可以表示氢原子,任选取代的烷基,环烷基,环烷基烷基,芳基,芳烷基,芳氧基烷基,芳族杂环基烷基或芳族杂环烷基 基团或基团ZC(= O) - 或ZSO 2 - ,当n表示1时,R 1表示任选取代的烷基,苄基, 苯乙基,1-萘基甲基,2-萘基甲基或吡啶-3-基甲基及其药学上可接受的盐具有药理学性质。