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Vadimezan的简便合成 被引量:2

A Concise Synthesis of Vadimezan
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摘要 2-氨基-3,4-二甲基苯甲酸经重氮化、溴代得到2-溴-3,4-二甲基苯甲酸,再与邻羟基苯乙酸醚化和在多聚磷酸中发生分子内傅-克酰化反应制得vadimezan,总收率为59%。 Vadimezan was synthesized from the diazotization and bromination of 2-amino-3,4-dimethylbenzoic acid, followed by etherification with 2-hydroxyphenylacetic acid, and intramolecular Friedel-Crafts acylation in polyphosphoric acid with a total yield of 59 %.
作者 刘学峰
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2015年第3期238-239,244,共3页 Chinese Journal of Pharmaceuticals
关键词 vadimezan 肿瘤血管阻断剂 合成 vadimezan tumor vascular disrupting agent synthesis
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