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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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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. |
format | Online Article Text |
id | pubmed-6641228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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