4.8 Article

General and Scalable Amide Bond Formation with Epimerization-Prone Substrates Using T3P and Pyridine

Journal

ORGANIC LETTERS
Volume 13, Issue 19, Pages 5048-5051

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol201875q

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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.

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