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钯催化 Catellani 反应的脱羧炔基终止:通过邻位 C-H 胺化和炔基化反应的简便合成α-炔基苯胺。

Decarboxylative Alkynyl Termination of Palladium-Catalyzed Catellani Reaction: A Facile Synthesis of α-Alkynyl Anilines via Ortho C-H Amination and Alkynylation.

机构信息

Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, China.

出版信息

Org Lett. 2015 May 1;17(9):2222-5. doi: 10.1021/acs.orglett.5b00830. Epub 2015 Apr 22.

Abstract

A palladium-catalyzed synthesis of α-alkynyl anilines is reported. The reaction proceeds via Catellani ortho C-H amination followed by decarboxylative alkynylative amination. Different terminal alkyne precursors were screened, and it was found that alkynyl carboxylic acids were superior over other alkynes, which led to operationally simple reaction conditions (no gradual addition of alkynes) and broad substrate scope. The reactivity of three different components matched well; as a result, relatively higher reaction temperature could be used, greatly shortening the reaction time to 4 h from the previously reported 144 h.

摘要

报道了钯催化的α-炔基苯胺的合成方法。该反应通过 Catellani 邻位 C-H 胺化反应,然后脱羧炔基化胺化反应进行。筛选了不同的末端炔烃前体,发现炔基羧酸优于其他炔烃,这使得反应条件操作简单(无需逐渐添加炔烃),底物范围广泛。三种不同组分的反应活性匹配良好;因此,可以使用相对较高的反应温度,将反应时间从之前报道的 144 小时大大缩短至 4 小时。

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