In(OTf)3 catalysed an expeditious synthesis of β-carboline-imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrazine conjugates

beta-Carboline containing alkaloids are ubiquitously present in Nature, while imidazo[1,2-a]pyridine nucleus is incorporated in various synthetic commercial drugs and biologically previliged moieties. On this basis, new beta-carboline-imidazoazine conjugates were designed and a small library of compounds integrating both the pharmacophores was constructed with 4-points of diversity by using the In(OTf)(3) assisted Groebke-Blackburn-Bienayme multicomponent strategy. The methodology was found to be simple and convenient for the efficient syntheses of beta-carboline-imidazo[1,2-a]azine conjugates. The present synthetic protocol provides several advantages like operational simplicity, appreciable atom economy, short reaction time and easy purification procedure.