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1H和13C核磁共振鉴定1,5-苯并二氮杂卓衍生物合成中意外生成的3,4-二氢喹喔啉。

1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives.

作者信息

Tjiou E M, Lhoussaine E G, Virieux D, Fruchier A

机构信息

Département de Chimie, Faculté des Sciences, Université Mohammed V, Rabat, Morocco.

出版信息

Magn Reson Chem. 2005 Jul;43(7):557-62. doi: 10.1002/mrc.1593.

Abstract

The reaction between o-phenylenediamines, dehydroacetic acid and aromatic aldehydes is shown to give not only the expected 1,5-benzodiazepine derivative but also a 3,4-dihydroquinoxaline, the structure of which was determined by its 1H and 13C 1D and 2D NMR spectra.

摘要

邻苯二胺、脱氢乙酸与芳香醛之间的反应表明,不仅生成了预期的1,5-苯并二氮杂䓬衍生物,还生成了一种3,4-二氢喹喔啉,其结构通过1H和13C一维及二维核磁共振谱确定。

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