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铜催化的通过 Ullmann 型偶联和有氧氧化合成喹唑啉衍生物。

Copper-catalyzed synthesis of quinazoline derivatives via Ullmann-type coupling and aerobic oxidation.

机构信息

Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, People's Republic of China.

出版信息

J Org Chem. 2010 Nov 19;75(22):7936-8. doi: 10.1021/jo101685d. Epub 2010 Oct 22.

Abstract

A simple and efficient copper-catalyzed approach to quinazoline derivatives has been developed, and the protocol uses readily available substituted (2-bromophenyl)methylamines and amides as the starting materials, and the cascade reactions were performed under air via sequential Ullmann-type coupling and aerobic oxidation without addition of any ligand or additive. The present method provides a convenient and practical strategy for synthesis of quinazoline derivatives.

摘要

一种简单高效的喹唑啉衍生物合成方法已经被开发出来,该方法使用易得的取代(2-溴苯基)甲胺和酰胺作为起始原料,通过连续的Ullmann 型偶联和有氧氧化反应在空气中进行级联反应,无需添加任何配体或添加剂。本方法为喹唑啉衍生物的合成提供了一种便捷实用的策略。

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