This method demonstrates regioselective trifluoromethylation in dihydropyrroloquinazolinones, indicating potential in pharmaceutical chemistry.
A visible-light-induced radical relay trifluoromethylation/cyclization reaction between N-cyano-N-isopentenyl arylamide or (E)-N-cinnamyl-N-cyanoarylamide with CF3Br has been developed, affording trifluoromethylated dihydropyrroloquinazolinone derivatives in good yields. A key feature of this method is the regioselective addition of the trifluoromethyl radical to the internal C=C bond of N-cyano-N-isopentenyl arylamides and (E)-N-cinnamyl-N-cyanoarylamides, which directly incorporates a trifluoromethyl group into the pyrrolidine ring of the dihydropyrroloquinazolinones. Mechanistic studies suggest a radical-mediated pathway. The broad substrate scope, excellent functional group tolerance, and use of green energy are expected to enhance its potential applications in pharmaceutical chemistry.
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Zhou et al. (2025) studied this question.