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5-异喹啉乙酰胺的合成

Synthesis of 5-Isoquinolineacetamide
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摘要 以5-溴异喹啉为原料,经醛基化、还原、溴化及氰基化反应制得5-(氰基甲基)异喹啉(5);5在酸作用下经水解合成了抗肿瘤药物咔唑糖苷的关键中间体——5-异喹啉乙酰胺,总收率28.7%,其结构经1H NMR和13C NMR确证。 5-Aeetonitrileisoquinoline (5) was prepared from 5-bromoisoquinoline by formation of alde- hyde group, reduction, bromination and eyanation. The important intermediate of antitumor drug carbazole glycosides, 5-isoquinolineacetamide, was synthesized in overall yield of 28.7% by hydrolysis of 5. The structure was confirmed by 1H NMR and 13C NMR.
机构地区 复旦大学药学院
出处 《合成化学》 CAS CSCD 北大核心 2013年第3期358-360,共3页 Chinese Journal of Synthetic Chemistry
基金 国家海洋863计划资助项目(2011AA09070105) 中国科学院上海药物研究所新药研究国家重点实验室开放课题(SIMM0812KF-08)
关键词 吲哚 咔唑 5-异喹啉乙酰胺 中间体 药物合成 indole carbazole 5-isoquinolineacetamide intermediate drug synthesis
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