Issue 36, 2024

Copper-promoted ortho-directed C–H amination of 2-arylpyridines with NH-heterocycles

Abstract

Copper-mediated C–N coupling of azaheterocycles with aryl C–H bonds has been realized for the synthesis of N-(hetero)arylated heteroarenes. This method is characterized by high regioselectivity, atom economy and a wide substrate scope of 2-arylazines and azaheterocycles. The corresponding C–N coupling products were shown to undergo further transformation to synthesize more complex molecules.

Graphical abstract: Copper-promoted ortho-directed C–H amination of 2-arylpyridines with NH-heterocycles

Supplementary files

Article information

Article type
Paper
Submitted
06 Jul 2024
Accepted
15 Aug 2024
First published
18 Aug 2024

Org. Biomol. Chem., 2024,22, 7390-7394

Copper-promoted ortho-directed C–H amination of 2-arylpyridines with NH-heterocycles

Y. Zeng and L. Dong, Org. Biomol. Chem., 2024, 22, 7390 DOI: 10.1039/D4OB01126K

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