Practical Synthesis of Allylic Heteroaromatic Amines via Pd‐Catalyzed Oxidative Amination of Olefins

Abstract Heteroaryl amines are prone to over coordination in the transition metal‐catalyzed olefin oxidation reaction system, which hinders the smooth catalytic reaction. Herein, we report a general method for the direct C─N coupling between inactive olefins and primary and secondary heterocyclic aromatic amines under palladium catalysis, which is an important transition that has not yet been revealed. By employing commercially available palladium catalysts, quinone oxidants, and inexpensive monodentate phosphine ligands, the oxidative amination of diverse heteroaryl amines proceeds smoothly, delivering a broad range of allyl heteroaryl amines with excellent regio‐ and stereoselectivity. Notably, this strategy enables the late‐stage modification of challenging biologically relevant molecules such as adenine and adenosine, further highlighting the practicality and synthetic utility of this reaction.

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Publication Details

Journal
Angewandte Chemie
Published
2025-12-18
DOI
https://doi.org/10.1002/ange.202520265
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Practical Synthesis of Allylic Heteroaromatic Amines via Pd‐Catalyzed Oxidative Amination of Olefins

Mingda Li, Wanqing Wu, Huanfeng Jiang, Yangbin Jin et al.
Angewandte Chemie
Catalytic C–H Functionalization Methods
article

Practical Synthesis of Allylic Heteroaromatic Amines via Pd‐Catalyzed Oxidative Amination of Olefins

Mingda Li, Wanqing Wu, Huanfeng Jiang, Yangbin Jin, Jiarui Li, Yupeng Chen
article en

Abstract

Abstract Heteroaryl amines are prone to over coordination in the transition metal‐catalyzed olefin oxidation reaction system, which hinders the smooth catalytic reaction. Herein, we report a general method for the direct C─N coupling between inactive olefins and primary and secondary heterocyclic aromatic amines under palladium catalysis, which is an important transition that has not yet been revealed. By employing commercially available palladium catalysts, quinone oxidants, and inexpensive monodentate phosphine ligands, the oxidative amination of diverse heteroaryl amines proceeds smoothly, delivering a broad range of allyl heteroaryl amines with excellent regio‐ and stereoselectivity. Notably, this strategy enables the late‐stage modification of challenging biologically relevant molecules such as adenine and adenosine, further highlighting the practicality and synthetic utility of this reaction.

Angewandte ChemieVol. 138(6)
Key Laboratory of Guangdong Province (CN), South China University of Technology (CN)
Openalex Percentile: Top 69%
Catalytic C–H Functionalization Methods
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