首页> 外文期刊>Advanced synthesis & catalysis >Efficient Copper-Catalyzed Synthesis of N-Alkylanthranilic Acids via an ortho-Substituent Effect of the Carboxyl Group of 2-Halo- benzoic Acids at Room Temperature
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Efficient Copper-Catalyzed Synthesis of N-Alkylanthranilic Acids via an ortho-Substituent Effect of the Carboxyl Group of 2-Halo- benzoic Acids at Room Temperature

机译:室温下2-卤代苯甲酸的羧基邻位取代作用对铜的催化合成N-烷基邻氨基苯甲酸

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摘要

We have developed an efficient copper-catalyzed method for the synthesis of N-alkylanthranilic acids. The protocol uses inexpensive copper(I) iodide/racemic 1,1'-binaphthyl-2,2'-diol (rac-BINOL) as the catalyst/ligand system, readily available 2-halobenzoic acids and aliphatic amines as the start- ing materials, the coupling reactions were performed at room temperature, and various functionalities in the substrates were tolerated.
机译:我们已经开发出一种用于合成N-烷基邻氨基苯甲酸的高效铜催化方法。该方案使用廉价的碘化铜(I)/外消旋1,1'-联萘-2,2'-二醇(rac-BINOL)作为催化剂/配体体系,现成的2-卤代苯甲酸和脂肪族胺作为起始原料在室温下进行偶联反应,并且可以耐受基质中的各种功能。

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