Litcius/Paper detail

Sustainable Synthetic Approaches for 3‐Aminoimidazo‐fused Heterocycles <i>via</i> Groebke‐Blackburn‐Bienaymé Process

Sivagami Mathavan, Y. B. R. D. Rajesh

2020ChemistrySelect12 citationsDOI

Abstract

Abstract Two different sustainable and efficient synthetic methods have been developed for the synthesis of a variety of 3‐aminoimidazo fused heterocycles by one‐pot three component reaction of 2‐aminoazines, aldehydes and isocyanides. The methods adopted were (a) aqueous micellar mediated condition (method A) (b) VB 1 catalyzed reaction under solvent‐free condition (method B). Excellent yields were obtained for a broad range of biologically significant imidazopyridine core molecules under green conditions at room temperature. Synthesis in aqueous micellar medium, mild reaction conditions, organocatalyst, easy work‐up and isolation, and gram scale synthesis, are some of the advantages of these protocols.

Topics & Concepts

ChemistryCombinatorial chemistryReaction conditionsAqueous solutionImidazopyridineGreen chemistrySolventAqueous mediumOrganic chemistryCatalysisReaction mechanismMulticomponent Synthesis of HeterocyclesChemistry and Chemical EngineeringSynthesis and biological activity
Sustainable Synthetic Approaches for 3‐Aminoimidazo‐fused Heterocycles <i>via</i> Groebke‐Blackburn‐Bienaymé Process | Litcius