Chloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo[1,2-]pyridines

A palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically potent 2-amidoimidazopyridine scaffolds. The aminocarbonylation reaction was found to be general with a range of amines and substituted imidazopyridines. Prelim...

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Veröffentlicht in:Organic & biomolecular chemistry 2018-09, Vol.16 (35), p.643-6437
Hauptverfasser: Nitha, P. R, Joseph, Manu M, Gopalan, Greeshma, Maiti, Kaustabh Kumar, Radhakrishnan, K. V, Das, Parthasarathi
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container_end_page 6437
container_issue 35
container_start_page 643
container_title Organic & biomolecular chemistry
container_volume 16
creator Nitha, P. R
Joseph, Manu M
Gopalan, Greeshma
Maiti, Kaustabh Kumar
Radhakrishnan, K. V
Das, Parthasarathi
description A palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically potent 2-amidoimidazopyridine scaffolds. The aminocarbonylation reaction was found to be general with a range of amines and substituted imidazopyridines. Preliminary biological evaluation of cytotoxicity on selected examples provides scope for future investigations. A palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically active 2-amidoimidazopyridine scaffolds.
doi_str_mv 10.1039/c8ob01486h
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Amines
Carbon monoxide
Chemical synthesis
Chloroform
Cytotoxicity
Palladium
Pyridines
Toxicity
title Chloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo[1,2-]pyridines
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