Catalyst-Free Regioselective C-3 Thiocyanation of Imidazopyridines

Imidazopyridine Surface Modification Reaction conditions
DOI: 10.1021/acs.joc.5b01637 Publication Date: 2015-10-02T17:20:41Z
ABSTRACT
A direct and straightforward approach for highly regioselective thiocyanation of imidazoheterocycles through sp2 C–H functionalization has been realized at room temperature. Various C-3 thiocyanated imidazopyridines are formed in moderate to good yield. The present method exhibits a mild selective access variety imidazopyridine derivatives pharmacological interest.
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