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Short Synthesis of Molnupiravir (EIDD-2801) via a Thionated Uridine Intermediate
[Image: see text] Molnupiravir (MK-4482, EIDD-2801) is an experimental drug that has been demonstrated to be effective for the treatment of COVID-19 in human clinical trials. Herein, we report a concise synthesis of the drug via a novel thionated derivative that relies on one-pot methodologies, thus...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552467/ https://www.ncbi.nlm.nih.gov/pubmed/34723033 http://dx.doi.org/10.1021/acsomega.1c04550 |
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author | Dey, Raghunath Nayak, Sourav Das, Parthasarathi Yadav, Somnath |
author_facet | Dey, Raghunath Nayak, Sourav Das, Parthasarathi Yadav, Somnath |
author_sort | Dey, Raghunath |
collection | PubMed |
description | [Image: see text] Molnupiravir (MK-4482, EIDD-2801) is an experimental drug that has been demonstrated to be effective for the treatment of COVID-19 in human clinical trials. Herein, we report a concise synthesis of the drug via a novel thionated derivative that relies on one-pot methodologies, thus decreasing the number of purification steps required. This route provides the drug in an overall 62% yield and >99% purity and uses cheap and readily available bulk chemicals, thereby providing an affordable synthesis of the drug for cheaper and wider global accessibility. |
format | Online Article Text |
id | pubmed-8552467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85524672021-10-29 Short Synthesis of Molnupiravir (EIDD-2801) via a Thionated Uridine Intermediate Dey, Raghunath Nayak, Sourav Das, Parthasarathi Yadav, Somnath ACS Omega [Image: see text] Molnupiravir (MK-4482, EIDD-2801) is an experimental drug that has been demonstrated to be effective for the treatment of COVID-19 in human clinical trials. Herein, we report a concise synthesis of the drug via a novel thionated derivative that relies on one-pot methodologies, thus decreasing the number of purification steps required. This route provides the drug in an overall 62% yield and >99% purity and uses cheap and readily available bulk chemicals, thereby providing an affordable synthesis of the drug for cheaper and wider global accessibility. American Chemical Society 2021-10-11 /pmc/articles/PMC8552467/ /pubmed/34723033 http://dx.doi.org/10.1021/acsomega.1c04550 Text en © 2021 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 | Dey, Raghunath Nayak, Sourav Das, Parthasarathi Yadav, Somnath Short Synthesis of Molnupiravir (EIDD-2801) via a Thionated Uridine Intermediate |
title | Short Synthesis of Molnupiravir (EIDD-2801) via a
Thionated Uridine Intermediate |
title_full | Short Synthesis of Molnupiravir (EIDD-2801) via a
Thionated Uridine Intermediate |
title_fullStr | Short Synthesis of Molnupiravir (EIDD-2801) via a
Thionated Uridine Intermediate |
title_full_unstemmed | Short Synthesis of Molnupiravir (EIDD-2801) via a
Thionated Uridine Intermediate |
title_short | Short Synthesis of Molnupiravir (EIDD-2801) via a
Thionated Uridine Intermediate |
title_sort | short synthesis of molnupiravir (eidd-2801) via a
thionated uridine intermediate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552467/ https://www.ncbi.nlm.nih.gov/pubmed/34723033 http://dx.doi.org/10.1021/acsomega.1c04550 |
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