Cobalt-catalyzed reductive carboxylation of pyridines with CO2via pyridylphosphonium salts

Abstract

Reports on late-stage C–H bond carboxylation reactions using CO2 are very limited. In this work, a cobalt-catalyzed carboxylation reaction of pyridylphosphonium salts with CO2 has been developed. The catalyst system consisting of Co(acac)2 and Mn is convenient and practical. When combined with triphenylphosphonation of the C4–H bond of pyridines, the formal C4–H carboxylation of pyridines with CO2 can be achieved via a one-pot, two-step procedure. This method has been further applied to the late-stage C–H bond carboxylation modifications of pyridine-containing drug molecules, such as loratadine.

Graphical abstract: Cobalt-catalyzed reductive carboxylation of pyridines with CO2 via pyridylphosphonium salts

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Article information

Article type
Communication
Submitted
08 Apr 2026
Accepted
28 Apr 2026
First published
29 Apr 2026

Org. Biomol. Chem., 2026, Advance Article

Cobalt-catalyzed reductive carboxylation of pyridines with CO2 via pyridylphosphonium salts

Y. Zhao, H. Wu, S. Tang, B. Li and B. Wang, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00565A

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