Electrochemically Enabled Direct C3-Formylation of Imidazopyridines with Me3 N as a Carbonyl Source
Zhicong Tang1, Gang Hong1, Shiyun Sun1
1Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, 200237, Shanghai, P. R. China.
Abstract:
A metal-free and oxidant-free electrochemically enabled strategy for C-3 formylation of imidazopyridines using trimethylamine as a one-carbon source has been established. This conversion has high functional group compatibility under mild conditions and ensures late-stage functionalization of pharmaceutical molecules. Furthermore, unexpected hexafluoroisopropoxylation products have been observed in some cases. Mechanistic studies using cyclic voltammetry and control experiments reveal the key intermediate of the formylation process.
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