A practical
and scalable protocol for electrochemical arylation
of quinoxalin(on)es with arylhydrazine hydrochlorides under mild conditions
has been developed. This method exhibits high efficiency, easy scalability,
and broad functional group tolerance. Various quinoxalin(on)es and
arylhydrazines underwent this transformation smoothly in an undivided
cell, providing the corresponding aryl-substituted quinoxalin(on)es
in moderate to good yields. A radical mechanism is involved in this
arylation reaction