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使用 T3P 和吡啶实现易差向异构化底物的通用和规模化酰胺键形成。

General and scalable amide bond formation with epimerization-prone substrates using T3P and pyridine.

机构信息

Chemical Research and Development, Pfizer Worldwide Research and Development, Eastern Point Road, Groton, Connecticut 06340, USA.

出版信息

Org Lett. 2011 Oct 7;13(19):5048-51. doi: 10.1021/ol201875q. Epub 2011 Aug 29.

Abstract

The mild combination of T3P (n-propanephosphonic acid anhydride) and pyridine has been developed for low-epimerization amide bond formation and implemented for the synthesis of a key intermediate to a glucokinase activator. This robust method is general for the coupling of various racemization-prone acid substrates and amines, including relatively non-nucleophilic anilines, and provides amides in high yields with very low epimerization. With easy reaction setup and product isolation, this protocol offers several practical and experimental benefits.

摘要

已开发出温和的 T3P(正丙基亚膦酸酐)和吡啶组合,用于低外消旋酰胺键形成,并应用于葡萄糖激酶激活剂的关键中间体的合成。这种稳健的方法适用于各种易外消旋化的酸底物和胺的偶联,包括相对非亲核性的苯胺,并以非常低的外消旋化率提供高产率的酰胺。该方案具有易于反应设置和产物分离的特点,提供了几个实际和实验方面的优势。

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