Synthesis of a novel pyrrolo-[3,2- c]quinoline N-oxide by aza-Baylis–Hillman adduct of o-nitrobenzaldehyde

Abstract

A new and high yielding approach for the synthesis of a novel pyrrolo-[3,2- c]quinoline N-oxide is described. The key step consisted in the palladium-catalyzed reductive cyclization of an uncommon 3-ketopyrrole derivative of o-nitrobenzaldehyde, obtained in a straightforward manner through an aza-Baylis–Hillman/ring closing metathesis/aromatization reaction. A deoxygenation reaction of this novel pyrrolo-[3,2- c]quinoline N-oxide afforded a new substituted pyrrolo-[3,2- c]quinoline analogue.