An atom-economical and regioselective metal-free C-5 chalcogenation of 8-aminoquinolines under mild conditions. Issue 48 (3rd December 2019)

• Record Type: Journal Article
• Authors: Kumar, Vipin; Banert, Klaus; Ray, Devalina; Saha, Biswajit
• Is Part Of: Organic & biomolecular chemistry. Volume 17:Issue 48(2019)
• Page Start: 10245
• Page End: 10250
• Publication Date: 2019-12-03
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c9ob02235j
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : An ecofriendly, atom-economical, iodine-catalyzed, regioselective C-5 chalcogenation of 8-aminoquinolines and its application in the late stage derivatization of primaquine analogues under mild conditions has been established. Abstract : A general and simple metal-free protocol for expedient C–H functionalization leading to the regioselective generation of C-5 chalcogenated 8-aminoquinoline analogues in up to 90% yield at room temperature (25 °C) has been established. This methodology is an eco-friendly approach to the atom-economical utilization of diaryl/dialkyl chalcogenides for direct access to chalcogenated quinolines and is scalable to the gram scale without considerable decrease in the yield of the product. It represents a practical alternative to the existing metal-catalyzed functionalization of 8-aminoquinoline derivatives with broad functional group tolerance. The controlled experiments suggest that the reaction possibly proceeds through an ionic pathway at room temperature. Furthermore, the potentiality for the functionalization of free amines in chalcogenated-8-aminoquinolines provides an attractive perspective for further elaboration of the amine substituent through chemical manipulations. The applicability of the standardized method has been augmented through late-stage antimalarial drug diversification of primaquine analogues.