Suppr超能文献

α-1-去甲乙酰美沙多的合成。α-1-乙酰美沙多的简便N-去甲基化反应。

Synthesis of alpha-1-noracetylmethadol. A facile N-demethylation of alpha-1-acetylmethadol.

作者信息

Chatterjie N, Inturrisi C E

出版信息

J Med Chem. 1975 Jun;18(6):630-1. doi: 10.1021/jm00240a024.

Abstract

A facile N-demethylation of the narcotic analgesic, alpha-1-acetylmethadol, was accomplished by allowing it to react with mercuric acetate under reflux in dilute acetic acid. The product, alpha-1-noracetylmethadol, was isolated as the hydrochloride in 50% yield. Methadone, when allowed to react with mercuric acetate under the same conditions, did not undergo N-demethylation and was recovered unchanged.

摘要

通过使麻醉性镇痛药α-1-乙酰美沙多在稀醋酸中回流时与醋酸汞反应,实现了其简便的N-去甲基化。产物α-1-去甲乙酰美沙多以盐酸盐形式分离得到,产率为50%。美沙酮在相同条件下与醋酸汞反应时,未发生N-去甲基化,且原样回收。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验