Chatterjie N, Inturrisi C E
J Med Chem. 1975 Jun;18(6):630-1. doi: 10.1021/jm00240a024.
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.
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。