Transition-metal-free synthesis of bipyridines from pyridyl pyrimidylsulfones

Abstract

We report a transition-metal-free cross-coupling of readily accessible pyridyl pyrimidylsulfones with azaaryl Grignard reagents that provides direct access to diverse bis-azaaryl products, including 2,2′-, 2,3′-, and 2,4′-bipyridines, under mild conditions, while also accommodating related azaaryl–heteroaryl products. The reaction proceeds through SNAr activation of the pyrimidylsulfone to generate magnesium pyridyl sulfinates in situ, followed by desulfinative C–C bond formation. The synthetic utility of the method is demonstrated by regiodivergent access to bipyridines and the preparation of caerulomycin F.

Graphical abstract: Transition-metal-free synthesis of bipyridines from pyridyl pyrimidylsulfones

Supplementary files

Article information

Article type
Research Article
Submitted
14 Mar 2026
Accepted
05 May 2026
First published
11 May 2026

Org. Chem. Front., 2026, Advance Article

Transition-metal-free synthesis of bipyridines from pyridyl pyrimidylsulfones

H. Kim, Y. Jin, S. Kim and J. Sohn, Org. Chem. Front., 2026, Advance Article , DOI: 10.1039/D6QO00332J

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