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A process for the preparation of derivatives of beta- (benzothiazolylthio) -and beta- (bencimidazoliltio) -carboxi- lic

机译:制备β-(苯并噻唑基硫代)-和β-(苯并咪唑酮)-羧酸衍生物的方法

摘要

The reaction of 2-mercapto-benzothiazole or -benzimidazole with alpha , beta -unsaturated carboxylic acid derivatives in a strongly acid reaction medium gives compounds of the formula I IMAGE I in which X is sulfur or NH, each radical R independently of one another is H, alkyl, halogenalkyl, alkoxy, alkylthio, alkylsulfonyl, phenyl, alkylphenyl, phenylalkyl, cycloalkyl, halogen, NO2, CN, COOH, COOalkyl or a tertiary amino or carbamoyl group and R1, R2 and R3 independently of one another are H, alkyl, halogenalkyl, hydroxyalkyl, alkoxyalkyl unesterified or esterified carboxyl or carboxylalkyl, carbamyol, carbamyolalkyl or unsubstituted or substituted aryl or aralkyl, or R1 and R2 together are straight-chain or branched alkylene, which can be substituted by 1 or 2 carboxyl groups, R4 is unsubstituted or substituted amino, alkoxy, cycloalkoxy, aryloxy or aralkyloxy, or R2 and R4 together are CH2-CO-O- or -CH2CO-NR5- or R3 and R4 together are -CO-O- or -CO-NR5-, forming an anhydride or imide ring, wherein R5 is unsubstituted or substituted alkyl, cycloalkyl, aryl, aralkyl or hydrogen.
机译:2-巯基-苯并噻唑或-苯并咪唑与α,β-不饱和羧酸衍生物在强酸反应介质中的反应得到式I I的化合物,其中X是硫或NH,每个基团R独立于一个另一个是H,烷基,卤代烷基,烷氧基,烷硫基,烷基磺酰基,苯基,烷基苯基,苯基烷基,环烷基,卤素,NO2,CN,COOH,COO烷基或叔氨基或氨基甲酰基,并且R1,R2和R3彼此独立地为H ,烷基,卤代烷基,羟烷基,烷氧基烷基未酯化或酯化的羧基或羧基烷基,氨基甲酚,氨基甲酚烷基或未取代或取代的芳基或芳烷基,或者R1和R2一起是直链或支链亚烷基,可以被1个或2个羧基取代, R 4是未取代或取代的氨基,烷氧基,环烷氧基,芳氧基或芳烷氧基,或R 2和R 4一起是CH 2 -CO-O-或-CH 2 CO-NR 5-或R 3和R 4一起是-CO-O-或-CO-NR 5-。 ,形成酸酐或酰亚胺环,其中R 5是未取代或取代的烷基,环烷基,芳基,芳烷基或氢。

著录项

  • 公开/公告号ES543005A0

    专利类型

  • 公开/公告日1985-12-16

    原文格式PDF

  • 申请/专利权人 CIBA GEIGY AG;

    申请/专利号ES19850543005

  • 发明设计人

    申请日1985-05-10

  • 分类号C07D235/28;C07D277/74;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:49

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