首页> 外国专利> N-acylate derivatives of anti-ulcerative omeprazole, its preparation method, and its preparation method using omeprazole

N-acylate derivatives of anti-ulcerative omeprazole, its preparation method, and its preparation method using omeprazole

机译:抗溃疡性奥美拉唑的N-酰化物衍生物,其制备方法和使用奥美拉唑的制备方法

摘要

The present invention relates to an N-acylate derivative (I) of omeprazole, a process for preparing the same, and a process for preparing omeprazole used as a therapeutic agent for ulcers using the same. I);(Wherein, " R " represents a functional group selected from a hydrogen atom, methyl, chloromethyl, trichloromethyl, bromomethyl, phenylmethyl or phenoxymethyl);Reacting 2-chloromethyl-3,5-dimethyl-4-methoxypyridine (II) with N-acyl-5-methoxy-2-mercaptobenzimidazole (III) to obtain thioether , And oxidizing the thioether (IV).;When the omeprazole is prepared by using the process for producing the N-acylate derivative (I) of the present invention, there is no by-product as in the case of reacting chloromethylpyridine with N-acylbenzimidazole, Which is easily separated, and a high purity compound can be produced by using the hydrolysis method using an enzyme.
机译:奥美拉唑的N-酰化物衍生物(I),其制备方法以及使用该化合物的溃疡制备用奥美拉唑的制备方法技术领域I);(其中,“ R”表示选自氢原子,甲基,氯甲基,三氯甲基,溴甲基,苯甲基或苯氧基甲基的官能团); 2-氯甲基-3,5-二甲基-4-甲氧基吡啶(II) N-酰基-5-甲氧基-2-巯基苯并咪唑(III)获得硫醚,并氧化硫醚(IV)。当使用本发明的N-酰化物衍生物(I)的制备方法制备奥美拉唑时与氯甲基吡啶与容易分离的N-酰基苯并咪唑反应的情况下不存在副产物,通过使用酶的水解方法可以制造高纯度的化合物。

著录项

  • 公开/公告号KR930023361A

    专利类型

  • 公开/公告日1993-12-18

    原文格式PDF

  • 申请/专利权人 손성배;

    申请/专利号KR19920009400

  • 申请日1992-05-30

  • 分类号C07D401/12;

  • 国家 KR

  • 入库时间 2022-08-22 04:38:23

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