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PROCESS FOR THE PREPARATION OF SALICYLIC DERIVATIVES OF N-ACETYL CYSTEINE

机译:N-乙酰半胱氨酸水杨酸衍生物的制备方法

摘要

S-salicylyl-N-acetylcysteine of formula (I) is prepared by reacting N-acetylcystine and salicylic acid as in the following, (A), The reactive deriv. selected from the salts of acetylsalicylic acid or mixed anhidrides is reacted with ethylchloroformate. (B), This product is reacted with N-acetylcysteine at low temp. in the presence of organic or inorganic base. (C), After the produced thioester is isolated, this is converted to their organic or inorganic salts in the hydrophillic, alcoholic or ketonic solvents. In (I), X is hydrogen, alkali metal, alkali earth metal or organic base. (I) is useful for antipyretics, antiinflammatories, analgesics and mucolytics.
机译:式(I)的S-水杨基-N-乙酰基半胱氨酸通过如下使(N)的N-乙酰基胱氨酸与水杨酸反应而制备,反应性衍生物。选自乙酰水杨酸的盐或混合的酸酐的盐与氯甲酸乙酯反应。 (B),该产物在低温下与N-乙酰半胱氨酸反应。在有机或无机碱存在下。 (C),分离出生成的硫酯后,将其在亲水,醇或酮溶剂中转化为有机盐或无机盐。在(I)中,X是氢,碱金属,碱土金属或有机碱。 (I)可用于退烧药,消炎药,止痛药和粘液溶解剂。

著录项

  • 公开/公告号KR890000618B1

    专利类型

  • 公开/公告日1989-03-22

    原文格式PDF

  • 申请/专利权人 PIETRO LONARDI & C. S.P.A;

    申请/专利号KR19820005229

  • 发明设计人 PONCHIROLI OSVALDO;

    申请日1982-11-19

  • 分类号C07C153/11;C07C101/24;

  • 国家 KR

  • 入库时间 2022-08-22 06:33:37

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