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盐酸普罗帕酮的合成

Synthesis of Propafenone Hydrochloride
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摘要 苯酚和乙酸酐经酯化、重排、与苯甲醛缩合和催化还原得到2′-羟基二氢查尔酮,再经由环氧氯丙烷醚化、正丙胺胺化、盐酸成盐得到盐酸普罗帕酮,总收率为25%。 Propafenone hydrochloride was synthesized from phenol and acetic anhydride by esterification, Fries rearrangement, condensation with benzaldehyde and catalytic reduction to give 2'-hydroxydihydrochalcone, which was subjected to etherification with epichlorohydrin, amination with n-propylamine and HC1 salt formation with an overall yield of 25 %.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2009年第5期329-330,共2页 Chinese Journal of Pharmaceuticals
关键词 盐酸普罗帕酮 抗心律失常药 合成 propafenone hydrochloride antiarrhythmic synthesis
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