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Zinc Chloride-Catalyzed Synthesis of Carbamates: An Application for the Synthesis of the Anti-Alzheimer’s Drug Rivastigmine
[Image: see text] Herein, we report a synthetic protocol for the synthesis of carbamates by employing zinc chloride as a catalyst from carbamoyl chlorides and aromatic/aliphatic alcohols. The developed protocol successfully utilizes the gram-scale synthesis of the FDA-approved rivastigmine drug and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557893/ https://www.ncbi.nlm.nih.gov/pubmed/36249350 http://dx.doi.org/10.1021/acsomega.2c05350 |
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author | Gayke, Manoj Hirapara, Nirbhay Narode, Hanuman Bhosle, Siddhanath D. Bhosale, Rajesh S. Yadav, Jhillu Singh |
author_facet | Gayke, Manoj Hirapara, Nirbhay Narode, Hanuman Bhosle, Siddhanath D. Bhosale, Rajesh S. Yadav, Jhillu Singh |
author_sort | Gayke, Manoj |
collection | PubMed |
description | [Image: see text] Herein, we report a synthetic protocol for the synthesis of carbamates by employing zinc chloride as a catalyst from carbamoyl chlorides and aromatic/aliphatic alcohols. The developed protocol successfully utilizes the gram-scale synthesis of the FDA-approved rivastigmine drug and its derivative. The utility of zinc chloride over other catalysts such as zinc dust and zinc acetate exhibits a 49–87% yield of carbamates. |
format | Online Article Text |
id | pubmed-9557893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95578932022-10-14 Zinc Chloride-Catalyzed Synthesis of Carbamates: An Application for the Synthesis of the Anti-Alzheimer’s Drug Rivastigmine Gayke, Manoj Hirapara, Nirbhay Narode, Hanuman Bhosle, Siddhanath D. Bhosale, Rajesh S. Yadav, Jhillu Singh ACS Omega [Image: see text] Herein, we report a synthetic protocol for the synthesis of carbamates by employing zinc chloride as a catalyst from carbamoyl chlorides and aromatic/aliphatic alcohols. The developed protocol successfully utilizes the gram-scale synthesis of the FDA-approved rivastigmine drug and its derivative. The utility of zinc chloride over other catalysts such as zinc dust and zinc acetate exhibits a 49–87% yield of carbamates. American Chemical Society 2022-09-26 /pmc/articles/PMC9557893/ /pubmed/36249350 http://dx.doi.org/10.1021/acsomega.2c05350 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Gayke, Manoj Hirapara, Nirbhay Narode, Hanuman Bhosle, Siddhanath D. Bhosale, Rajesh S. Yadav, Jhillu Singh Zinc Chloride-Catalyzed Synthesis of Carbamates: An Application for the Synthesis of the Anti-Alzheimer’s Drug Rivastigmine |
title | Zinc Chloride-Catalyzed Synthesis of Carbamates: An
Application for the Synthesis of the Anti-Alzheimer’s Drug
Rivastigmine |
title_full | Zinc Chloride-Catalyzed Synthesis of Carbamates: An
Application for the Synthesis of the Anti-Alzheimer’s Drug
Rivastigmine |
title_fullStr | Zinc Chloride-Catalyzed Synthesis of Carbamates: An
Application for the Synthesis of the Anti-Alzheimer’s Drug
Rivastigmine |
title_full_unstemmed | Zinc Chloride-Catalyzed Synthesis of Carbamates: An
Application for the Synthesis of the Anti-Alzheimer’s Drug
Rivastigmine |
title_short | Zinc Chloride-Catalyzed Synthesis of Carbamates: An
Application for the Synthesis of the Anti-Alzheimer’s Drug
Rivastigmine |
title_sort | zinc chloride-catalyzed synthesis of carbamates: an
application for the synthesis of the anti-alzheimer’s drug
rivastigmine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557893/ https://www.ncbi.nlm.nih.gov/pubmed/36249350 http://dx.doi.org/10.1021/acsomega.2c05350 |
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