首页> 外国专利> 2-(@(3754/24)1H-BENZIMIDAZOL-2-YL)SULFINYLMETHYL)-4-SUBSTITUTED AMINO-5-PHRIMIDINECARBOXYLIC ACID DERIVATIVE

2-(@(3754/24)1H-BENZIMIDAZOL-2-YL)SULFINYLMETHYL)-4-SUBSTITUTED AMINO-5-PHRIMIDINECARBOXYLIC ACID DERIVATIVE

机译:2-(@(3754/24)1H-苯并咪唑-2-基)磺基亚甲基)-4-取代的氨基-5-嘧啶羧酸衍生物

摘要

PURPOSE: To provide the subject low toxic new compound having a combination of gastric acid secretion-inhibitory activity and digestive tract mucous membrane-protective activity, thus useful as an anti-digestive ulcerous agent. ;CONSTITUTION: The objective compound of formula I (R1 is N,N-dimethylammno, N-ethyl-N-methylammno or morpholmno; R2 is lower alkyl), e.g. 2-[(IH-benz imidazolk-2-yl)sulfinylmethyl]-4-dimethylamino-5-pyrimidinecarboxylic ethyl ester. The compound of the formula I can be obtained by oxidizing a compound of formula II with an oxidizing agent such as hydrogen peroxide, peracetic acid, or m-chloroperbenzoic acid.;COPYRIGHT: (C)1993,JPO&Japio
机译:目的:提供具有胃酸分泌抑制活性和消化道粘膜保护活性的组合的本发明的低毒新化合物,因此可用作抗消化性溃疡剂。 ;组成:式I的目标化合物(R 1 为N,N-二甲基氨气,N-乙基-N-甲基氨气或吗啉醇; R 2 为低级烷基),例如2-[((IH-苯并咪唑基-2-基)亚磺酰基甲基] -4-二甲基氨基-5-嘧啶羧酸乙酯。式Ⅰ化合物可通过用氧化剂如过氧化氢,过氧乙酸或间氯过苯甲酸氧化式Ⅱ化合物而制得。COPYRIGHT:(C)1993,JPO&Japio

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