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Manufacturing method of S- carboxymethyl -L- cysteine

机译:S-羧甲基-L-半胱氨酸的制备方法

摘要

PURPOSE:To obtain the above compound in high efficiency, by reacting L- cysteine in the presence of bisulfite ion under specific condition, reacting the produced L-cysteine with a monohalogenoacetic acid ester without separating from the reaction system and hydrolyzing the reaction product. CONSTITUTION:L-cysteine is made to react at pH6.0-5.5 at a temperature below boiling point in the presence of bisulfite ion to produce L-cysteine and S-sulfo-L-cysteine. Without separating the L-cysteine from the reaction liquid, the reaction products are made to react with a monohalogenoacetic acid at pH7.5-5 to selectively form S-carboxymethyl-L-cysteine from L-cysteine, the product is separated from the reaction liquid, and the S-sulfo-L-cysteine is hydrolyzed by reacting the motor liquor with a mineral acid. The produced L-cysteine is again used as a source of raw material. The objective compound useful as a synthetic raw material for pharmaceuticals such as a expectorant can be produced by this process economically at a low cost without using particular reaction apparatus.
机译:目的:通过在特定条件下使亚硫酸氢根离子存在下的L-半胱氨酸与L-半胱氨酸反应,使生成的L-半胱氨酸与单卤代乙酸酯反应,而不会从反应体系中分离出来并水解反应产物,从而高效地获得上述化合物。组成:在亚硫酸氢根离子存在下,使L-半胱氨酸在低于沸点的pH6.0-5.5下反应,生成L-半胱氨酸和S-磺基-L-半胱氨酸。在不从反应液中分离出L-半胱氨酸的情况下,使反应产物与pH7.5-5的单卤代乙酸反应,以从L-半胱氨酸选择性地形成S-羧甲基-L-半胱氨酸,将产物从反应中分离出来。液体,S-磺基-L-半胱氨酸通过使马达液体与无机酸反应而水解。产生的L-半胱氨酸再次用作原料来源。通过该方法,可以在不使用特定的反应装置的情况下以低成本经济地生产用作药物的合成原料的目标化合物,例如祛痰剂。

著录项

  • 公开/公告号JP2501852B2

    专利类型

  • 公开/公告日1996-05-29

    原文格式PDF

  • 申请/专利权人 SHOWA DENKO KK;

    申请/专利号JP19880017159

  • 发明设计人 UCHIJO SHUICHI;INOE OSAMI;

    申请日1988-01-29

  • 分类号C07C323/58;C07C319/14;

  • 国家 JP

  • 入库时间 2022-08-22 03:56:42

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