Electrochemically driven nickel catalysis for formal C–H amination

Gege Jiang, Yun Sa, Bingnan Wang, Duanyang Kong
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引用次数: 0

Abstract

The C–H amination of arenes represents a streamlined approach to arylamines, yet most existing methods rely on preactivated nitrogen reagents or directing groups, limiting practicality and substrate scope. Herein, we report a nickel-catalyzed electroreductive formal C–H amination of aryl bromides with secondary amines, enabling efficient access to 4-bromomorpholinobenzene derivatives. This halogen-enabled strategy allows formal C–H amination through transient bromine removal and reinstallation. The reaction employs electricity as a traceless redox reagent, proceeds under mild conditions without stoichiometric chemical oxidants, and exhibits broad functional group tolerance. Mechanistic studies suggest that the transformation involves electrochemically generated Ni(0) species and nitrogen-centered radicals, followed by nickel-mediated C–N bond formation and subsequent bromination. The synthetic utility of this protocol is demonstrated by gram-scale reactions, diverse downstream transformations, and a concise synthesis of the pharmaceutically relevant scaffold Entospletinib.
电化学驱动镍催化正态碳-氢胺化
芳烃的C-H胺化代表了芳胺的简化方法,但大多数现有方法依赖于预活化氮试剂或导向基团,限制了实用性和底物范围。在此,我们报道了镍催化芳基溴与仲胺的电还原形式C-H胺化,从而有效地获得了4-溴代喹啉苯衍生物。这种卤素激活策略允许通过瞬态溴去除和重新安装正式的碳氢胺化。该反应使用电作为无痕迹的氧化还原试剂,在温和的条件下进行,没有化学计量化学氧化剂,并表现出广泛的官能团耐受性。机理研究表明,该转变涉及电化学生成的Ni(0)物种和氮中心自由基,然后是镍介导的C-N键形成和随后的溴化。该方案的合成效用通过克级反应、不同的下游转化和药学相关支架Entospletinib的简明合成证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.80
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