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硼催化羧酸对胺的 N-烷基化反应。

Boron-Catalyzed N-Alkylation of Amines using Carboxylic Acids.

机构信息

iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei 230026 (China).

出版信息

Angew Chem Int Ed Engl. 2015 Jul 27;54(31):9042-6. doi: 10.1002/anie.201503879. Epub 2015 Jul 6.

Abstract

A boron-based catalyst was found to catalyze the straightforward alkylation of amines with readily available carboxylic acids in the presence of silane as the reducing agent. Various types of primary and secondary amines can be smoothly alkylated with good selectivity and good functional-group compatibility. This metal-free amine alkylation was successfully applied to the synthesis of three commercial medicinal compounds, Butenafine, Cinacalcet. and Piribedil, in a one-pot manner without using any metal catalysts.

摘要

研究发现,硼酸基催化剂在硅烷作为还原剂的存在下可以催化伯胺与易得羧酸的直接烷基化反应。各种类型的伯胺和仲胺都可以以良好的选择性和官能团兼容性顺利地进行烷基化反应。这种无金属的胺烷基化反应成功地应用于布替萘芬、西那卡塞和吡贝地尔三种商业药物化合物的一锅法合成中,无需使用任何金属催化剂。

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