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铜催化的2-卤代芳基三氮烯与叠氮化钠的串联环化反应:在水中选择性合成2H-苯并三唑

Copper-catalyzed cascade cyclization reaction of 2-haloaryltriazenes and sodium azide: selective synthesis of 2H-benzotriazoles in water.

作者信息

Shang Xiaobo, Zhao Shixian, Chen Wanzhi, Chen Chao, Qiu Huayu

机构信息

Department of Chemistry, Zhejiang University, Hangzhou 310028 (China), Fax: (+86) 571-88273314.

出版信息

Chemistry. 2014 Feb 10;20(7):1825-8. doi: 10.1002/chem.201303712. Epub 2014 Jan 21.

Abstract

A new approach to the synthesis of 2H-benzotriazoles is described. This strategy is based on the copper-catalyzed C-N coupling of 2-haloaryltriazenes or 2-haloazo compounds with sodium azide and the intramolecular addition of nitrene to N=N bonds. This approach allows the synthesis of various N-amino- and N-aryl-2H-benzotriazoles in water, in good to excellent yields. The procedure is simple and the starting materials and catalyst are easily available, offering a practical and convenient synthetic route to 2-substituted benzotriazoles.

摘要

描述了一种合成2H-苯并三唑的新方法。该策略基于铜催化的2-卤代芳基三氮烯或2-卤代偶氮化合物与叠氮化钠的C-N偶联以及氮烯分子内加成到N=N键上。这种方法能够在水中以良好至优异的产率合成各种N-氨基和N-芳基-2H-苯并三唑。该方法简单,起始原料和催化剂易于获得,为2-取代苯并三唑提供了一条实用且便捷的合成路线。

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