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三氟乙酸介导的 1,2,3-苯并三嗪-4(3H)-酮的脱氮-羟化反应:一种无金属方法。

Trifluoroacetic Acid-Mediated Denitrogenative -Hydroxylation of 1,2,3-Benzotriazin-4(3)-ones: A Metal-Free Approach.

机构信息

Department of Chemistry, SRM University, AP, Amaravati, Andhra Pradesh 522 502, India.

Department of Chemistry, SRM Institute of Science and Technology, Kattankulathur, Chennai 603 203, India.

出版信息

J Org Chem. 2022 Jul 1;87(13):8752-8756. doi: 10.1021/acs.joc.2c00354. Epub 2022 Jun 14.

Abstract

An efficient trifluoroacetic acid-mediated denitrogenative hydroxylation of 1,2,3-benzotriazin-4(3)-ones is described. This metal-free approach is compatible with a wide range of 1,2,3-benzotriazin-4(3)-ones, affording -hydroxylated benzamides in good to high yields with a short reaction time. The reaction is believed to proceed via a benzene diazonium intermediate. The synthetic utility of the reaction was successfully demonstrated by the preparation of an antimicrobial drug, Riparin C, and benzoxazine-2,4(3)-diones in good yields.

摘要

描述了一种高效的三氟乙酸介导的 1,2,3-苯并三嗪-4(3)-酮的脱氮羟化反应。这种无金属的方法与广泛的 1,2,3-苯并三嗪-4(3)-酮兼容,在短反应时间内以良好到高产率提供 -羟化苯甲酰胺。该反应被认为是通过苯重氮中间体进行的。该反应的合成实用性通过制备抗菌药物 Riparin C 和苯并恶嗪-2,4(3)-二酮以良好的产率得到了成功证明。

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