Author:
Dash Jyotirmayee,Basak Soumya Jyoti,Paul Pratap
Abstract
AbstractWe report an efficient synthesis of 6-substituted imidazo[2,1-b]thiazoles from 2-aminothiazoles and acetophenones through intramolecular cyclization of in situ generated thiazolium ylides. This one-pot cascade process efficiently forms two C–N bonds and is facilitated by both Cu(OTf)2/KI and FeCl3/ZnI2 systems. The method utilizes commercially available starting materials and features mild reaction conditions, tolerance to different functional groups, and ease of operation. The synthetic applicability has further been demonstrated through post-modification of imidazo[2,1-b]thiazole analogues.
Funder
Wellcome Trust DBT India Alliance
Department of Science and Technology, Ministry of Science and Technology, India
Council of Scientific and Industrial Research, India