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Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T

[Image: see text] An environment-friendly method for the chlorination of imidazoheterocycles has been developed using chloramine-T, a novel chlorinating reagent. A bunch of C-3 chloro-substituted imidazo[1,2-a]pyridines with variety of functionalities have been synthesized in good yields under neat...

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Autores principales: Dey, Amrita, Singsardar, Mukta, Sarkar, Rajib, Hajra, Alakananda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641228/
https://www.ncbi.nlm.nih.gov/pubmed/31458602
http://dx.doi.org/10.1021/acsomega.7b01844
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author Dey, Amrita
Singsardar, Mukta
Sarkar, Rajib
Hajra, Alakananda
author_facet Dey, Amrita
Singsardar, Mukta
Sarkar, Rajib
Hajra, Alakananda
author_sort Dey, Amrita
collection PubMed
description [Image: see text] An environment-friendly method for the chlorination of imidazoheterocycles has been developed using chloramine-T, a novel chlorinating reagent. A bunch of C-3 chloro-substituted imidazo[1,2-a]pyridines with variety of functionalities have been synthesized in good yields under neat condition at room temperature within very short time. This chlorination process is also applicable to imidazo[2,1-b]thiazole scaffolds. The present methodology is relevant to gram-scale synthesis. The major advantages of this system such as wide applicability, easy availability of reactants, open-air and metal- and solvent-free reaction conditions, no need of work-up, and simple purification technique represent a green synthetic protocol.
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spelling pubmed-66412282019-08-27 Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T Dey, Amrita Singsardar, Mukta Sarkar, Rajib Hajra, Alakananda ACS Omega [Image: see text] An environment-friendly method for the chlorination of imidazoheterocycles has been developed using chloramine-T, a novel chlorinating reagent. A bunch of C-3 chloro-substituted imidazo[1,2-a]pyridines with variety of functionalities have been synthesized in good yields under neat condition at room temperature within very short time. This chlorination process is also applicable to imidazo[2,1-b]thiazole scaffolds. The present methodology is relevant to gram-scale synthesis. The major advantages of this system such as wide applicability, easy availability of reactants, open-air and metal- and solvent-free reaction conditions, no need of work-up, and simple purification technique represent a green synthetic protocol. American Chemical Society 2018-03-26 /pmc/articles/PMC6641228/ /pubmed/31458602 http://dx.doi.org/10.1021/acsomega.7b01844 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Dey, Amrita
Singsardar, Mukta
Sarkar, Rajib
Hajra, Alakananda
Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title_full Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title_fullStr Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title_full_unstemmed Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title_short Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T
title_sort environment-friendly protocol for the chlorination of imidazoheterocycles by chloramine-t
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641228/
https://www.ncbi.nlm.nih.gov/pubmed/31458602
http://dx.doi.org/10.1021/acsomega.7b01844
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