Synthesis of substituted benzo[b][1,4]oxazepine derivatives by the reaction of 2-aminophenols with alkynones

被引:10
|
作者
Oshimoto, Kohei [1 ]
Zhou, Biao [1 ]
Tsuji, Hiroaki [1 ]
Kawatsura, Motoi [1 ]
机构
[1] Nihon Univ, Coll Humanities & Sci, Dept Chem, Setagaya Ku, Tokyo 1568550, Japan
基金
日本学术振兴会;
关键词
5-HT1A RECEPTOR AGONISTS; METAL-FREE SYNTHESIS; SMILES REARRANGEMENT; DIARYL ETHERIFICATION; HIGHLY-EFFICIENT; CYCLIZATION; UGI; DIBENZOXAZEPINONES; NITROGEN; PYRIDOBENZOXAZEPINONES;
D O I
10.1039/c9ob02450f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We have developed a novel synthetic method accessing benzo[b][1,4]oxazepines that are one of the rare classes of benzoxazepine derivatives by reaction of 2-aminophenols with alkynones in 1,4-dioxane at 100 degrees C. A series of benzo[b][1,4]oxazepine derivatives can be prepared by using this synthetic protocol. Mechanistic experiments indicated that the hydroxy proton of the aminophenol could play a crucial role in the formation of an alkynylketimine intermediate that undergoes 7-endo-dig cyclization.
引用
收藏
页码:415 / 419
页数:5
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