One-Pot Synthesis ofN-Substituted Diaza[12]annulenes

N-Substituted diaza[12]annulenes are obtained by one -pot reaction of N-(2,4-dinitrophenyl)pyridinium chloride with amines in moderate to high yields. The 1H NMR spectrum reveals that diamagnetic ring current is generated in the diaza[12]annulene ring. The N-substituted diaza[12]annulenes are electrochemically active in solution.