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通过铁催化的芳基酰胺与 N-氯代胺的邻位氨化反应合成邻氨基苯甲酸衍生物。

Synthesis of anthranilic acid derivatives through iron-catalyzed ortho amination of aromatic carboxamides with N-chloroamines.

机构信息

Department of Chemistry, School of Science, The University of Tokyo , 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

J Am Chem Soc. 2014 Jan 15;136(2):646-9. doi: 10.1021/ja412521k. Epub 2014 Jan 6.

Abstract

Arenes possessing an 8-quinolinylamide group as a directing group are ortho aminated with N-chloroamines and N-benzoyloxyamines in the presence of an iron/diphosphine catalyst and an organometallic base to produce anthranilic acid derivatives in high yield. The reaction proceeds via iron-catalyzed C-H activation, followed by the reaction of the resulting iron intermediate with N-chloroamine. The choice of the directing group and diphosphine ligand is crucial for obtaining the anthranilic acid derivative with high yield and product selectivity.

摘要

具有 8-喹啉酰胺基作为导向基团的芳基在铁/双膦催化剂和有机金属碱的存在下与 N-氯代胺和 N-苯甲酰氧基胺进行邻位胺化,以高产率得到邻氨基苯甲酸衍生物。该反应通过铁催化的 C-H 活化进行,然后是所得铁中间体与 N-氯代胺的反应。导向基团和双膦配体的选择对于获得高产率和产物选择性的邻氨基苯甲酸衍生物至关重要。

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