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2-(5-碘-1,2,3-三唑基)苯甲酸的环化引发脱氮转化反应

Annulation-Triggered Denitrogenative Transformations of 2-(5-Iodo-1,2,3-triazolyl)benzoic Acids.

作者信息

Voloshkin Vladislav A, Kotovshchikov Yury N, Latyshev Gennadij V, Lukashev Nikolay V, Beletskaya Irina P

机构信息

Chemistry Department, M. V. Lomonosov Moscow State University, 1/3 Leninskiye Gory, Moscow 119991, Russia.

出版信息

J Org Chem. 2022 Jun 3;87(11):7064-7075. doi: 10.1021/acs.joc.2c00235. Epub 2022 May 18.

Abstract

The ability of [1,2,3]triazolobenzoxazinones to act as a source of "hidden" diazo group was discovered. These diazo precursors can be easily prepared by the intramolecular cyclization of 2-(5-iodo-1,2,3-triazolyl)benzoic acids. The Cu-catalyzed capture of the hidden diazo group allows for further functionalization through the denitrogenative pathway. The transformations proceed the formation of either diazoimine or diazoamide intermediates. Novel routes to various anthranilamides as well as thiolated benzoxazinones were developed using the one-pot cyclization/diazo capture procedure.

摘要

发现了[1,2,3]三唑并苯并恶嗪酮作为“隐藏”重氮基团来源的能力。这些重氮前体可通过2-(5-碘-1,2,3-三唑基)苯甲酸的分子内环化轻松制备。铜催化的隐藏重氮基团捕获允许通过脱氮途径进行进一步功能化。转化过程中会形成重氮亚胺或重氮酰胺中间体。使用一锅环化/重氮捕获程序开发了制备各种邻氨基苯甲酰胺以及硫醇化苯并恶嗪酮的新路线。

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