作者:Darius Zlotos、Christian Markl
DOI:10.1055/s-0030-1258968
日期:2011.1
Agomelatine was synthesized from (2-methoxynaphthalene-8-yl)oxoacetic acid in a four-step approach involving borane reduction, semipinacol rearrangement of the resulting diol, aldoxime formation, and Ra-Ni hydrogenation/acetylation in 51% overall yield. The reaction sequence includes a novel one-pot conversion of an aldoxime into an N-acetylamine. The synthetic route could be useful as a new approach towards N-acetylarylethylamines.
阿戈美拉亭是通过四步法从(2-美氧萘-8-基)氧乙酸合成的,涉及硼烷还原、生成的二醇的半匹卡尔重排、醛肟形成以及Ra-Ni加氢/乙酰化,整体产率为51%。反应序列包括醛肟一锅法转化为N-乙酰氨基的创新方法。这一合成路线可能作为一种新方法,对N-乙酰芳基乙胺的合成具有潜在的应用价值。