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Scalable synthesis of favipiravir via conventional and continuous flow chemistry
Decagram scale synthesis of favipiravir was performed in 9 steps using diethyl malonate as cheap starting material. Hydrogenation and bromination steps were achieved by employing a continuous flow reactor. The synthetic process provided a total of 16% yield and it is suitable for larger-scale synthe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044180/ https://www.ncbi.nlm.nih.gov/pubmed/35493228 http://dx.doi.org/10.1039/d1ra06963b |
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author | Tiyasakulchai, Thanat Charoensetakul, Netnapa Khamkhenshorngphanuch, Thitiphong Thongpanchang, Chawanee Srikun, Onsiri Yuthavong, Yongyuth Srimongkolpithak, Nitipol |
author_facet | Tiyasakulchai, Thanat Charoensetakul, Netnapa Khamkhenshorngphanuch, Thitiphong Thongpanchang, Chawanee Srikun, Onsiri Yuthavong, Yongyuth Srimongkolpithak, Nitipol |
author_sort | Tiyasakulchai, Thanat |
collection | PubMed |
description | Decagram scale synthesis of favipiravir was performed in 9 steps using diethyl malonate as cheap starting material. Hydrogenation and bromination steps were achieved by employing a continuous flow reactor. The synthetic process provided a total of 16% yield and it is suitable for larger-scale synthesis and production. |
format | Online Article Text |
id | pubmed-9044180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90441802022-04-28 Scalable synthesis of favipiravir via conventional and continuous flow chemistry Tiyasakulchai, Thanat Charoensetakul, Netnapa Khamkhenshorngphanuch, Thitiphong Thongpanchang, Chawanee Srikun, Onsiri Yuthavong, Yongyuth Srimongkolpithak, Nitipol RSC Adv Chemistry Decagram scale synthesis of favipiravir was performed in 9 steps using diethyl malonate as cheap starting material. Hydrogenation and bromination steps were achieved by employing a continuous flow reactor. The synthetic process provided a total of 16% yield and it is suitable for larger-scale synthesis and production. The Royal Society of Chemistry 2021-12-01 /pmc/articles/PMC9044180/ /pubmed/35493228 http://dx.doi.org/10.1039/d1ra06963b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Tiyasakulchai, Thanat Charoensetakul, Netnapa Khamkhenshorngphanuch, Thitiphong Thongpanchang, Chawanee Srikun, Onsiri Yuthavong, Yongyuth Srimongkolpithak, Nitipol Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title | Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title_full | Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title_fullStr | Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title_full_unstemmed | Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title_short | Scalable synthesis of favipiravir via conventional and continuous flow chemistry |
title_sort | scalable synthesis of favipiravir via conventional and continuous flow chemistry |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044180/ https://www.ncbi.nlm.nih.gov/pubmed/35493228 http://dx.doi.org/10.1039/d1ra06963b |
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