Regioselective Direct C-H Trifluoromethylation of Pyridine.

A highly efficient and regioselective direct C-H trifluoromethylation of pyridine based on an N-methylpyridine quaternary ammonium activation strategy has been developed. A variety of trifluoromethylpyridines can be obtained in good yield and excellent regioselectivity by treating the pyridinium iodide salts with trifluoroacetic acid in the presence of silver carbonate in N,N-dimethylformamide. The protocol features good functional group compatibility, easily available starting materials, and operational simplicity. Controlled experiments showed that the reaction may involve a nucleophilic trifluoromethylation mechanism.