Visible Light Mediated External Oxidant Free Selective C5 Bromination of 8‐aminoquinoline Amides under Ambient Conditions

Selective functionalization of quinolines is the hot topic of organic synthesis due to its wide application in natural products, medicine, etc. In this research, C5 bromination of 8‐aminoquinoline amides have been achieved using the strategy of photoredox catalysis under mild conditions. Easily available 10‐phenylphenothiazine is employed as the organophotoredox catalyst and CBr4 is used as the bromine source. No external oxidant or transition metal catalyst is needed in this transformation. Both the alkyl and aryl substituted carboxamides are compatible with this method.