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盐酸噻氯匹定的合成 被引量:13

SYNTHESIS OF TICLOPIDINE HYDROCHLORIDE
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摘要 噻吩甲醛经与硝基甲烷缩合、还原、与甲醛缩合、环合制得主环4,5,6,7-四氢噻吩并[3,2-C]吡啶,然后用2-氯氯苄进行N-烃化、成盐制得盐酸噻氯匹定,总收率38.6%。 The new platelet aggregation inhibitor ticlopidine hydrochloride was synthesized from 2 thiophencarboxaldehyde through condensation with nitromethane,followed by reduction to give 2 (2 thienyl)ethylamine,which was reacted with formaldhyde,subsequent annulation and final condensation with 2 chlorobenzyl chloride.The reaction conditions were modified to give 38.6% overall yield.
作者 岑均达
出处 《中国医药工业杂志》 CAS CSCD 北大核心 1997年第5期197-199,共3页 Chinese Journal of Pharmaceuticals
关键词 血小板聚集抑制 盐酸噻氯匹定 四氢噻吩并 吡啶 platelet aggregation inhibitor,ticlopidne hydrochloride,4,5,6,7 tetrahydrothienopyridine,synthesis
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