CuI/2-Aminopyridine 1‑Oxide Catalyzed Amination of Aryl Chlorides with Aliphatic Amines

A class of 2-aminopyridine 1-oxides are discovered to be effective ligands for the Cu-catalyzed amination of less reactive (hetero)­aryl chlorides. A wide range of functionalized (hetero)­aryl chlorides reacted with various aliphatic amines to afford the desired products in good to excellent yields...

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Veröffentlicht in:Organic letters 2020-10, Vol.22 (19), p.7486-7490
Hauptverfasser: Liu, Wenjie, Xu, Jiamin, Chen, Xiahong, Zhang, Fuxing, Xu, Zhifeng, Wang, Deping, He, Yongqiang, Xia, Xiaohong, Zhang, Xin, Liang, Yun
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Sprache:eng
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Zusammenfassung:A class of 2-aminopyridine 1-oxides are discovered to be effective ligands for the Cu-catalyzed amination of less reactive (hetero)­aryl chlorides. A wide range of functionalized (hetero)­aryl chlorides reacted with various aliphatic amines to afford the desired products in good to excellent yields under the catalyst of CuI/2-aminopyridine 1-oxides. Furthermore, the catalyst system worked well for the coupling of cyclic secondary amines and N-methyl benzylamine with (hetero)­aryl chlorides.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.0c02672