Iridium-Catalyzed Asymmetric Reductive Amination of C2-Acylpyridines

Abstract

Chiral 1-pyridin-2-yl-ethylamines are significant building blocks for synthetic chemistry and pharmaceutical sciences, while their stereoselective and practical synthesis remains challenging and usually troublesome. Herein, we present a novel iridium-catalyzed direct asymmetric reductive amination of 2-acylpyridines with anilines, affording a series of chiral 1-pyridin-2-yl-ethylamines with up to 97% yield and 95% ee. A gram-scale reaction is also performed to demonstrate the practicality of this method.

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2025
Accepted
12 Aug 2025
First published
13 Aug 2025
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2025, Accepted Manuscript

Iridium-Catalyzed Asymmetric Reductive Amination of C2-Acylpyridines

G. Wang, Z. Nie, H. You and Q. Yin, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC04017E

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