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Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO
[Image: see text] Sulfonamides have played a defining role in the history of drug development and continue to be prevalent today. In particular, primary sulfonamides are common in marketed drugs. Here we describe the direct synthesis of these valuable compounds from organometallic reagents and a nov...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754190/ https://www.ncbi.nlm.nih.gov/pubmed/33237777 http://dx.doi.org/10.1021/acs.orglett.0c03505 |
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author | Davies, Thomas Q. Tilby, Michael J. Skolc, David Hall, Adrian Willis, Michael C. |
author_facet | Davies, Thomas Q. Tilby, Michael J. Skolc, David Hall, Adrian Willis, Michael C. |
author_sort | Davies, Thomas Q. |
collection | PubMed |
description | [Image: see text] Sulfonamides have played a defining role in the history of drug development and continue to be prevalent today. In particular, primary sulfonamides are common in marketed drugs. Here we describe the direct synthesis of these valuable compounds from organometallic reagents and a novel sulfinylamine reagent, t-BuONSO. A variety of (hetero)aryl and alkyl Grignard and organolithium reagents perform well in the reaction, providing primary sulfonamides in good to excellent yields in a convenient one-step process. |
format | Online Article Text |
id | pubmed-7754190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77541902020-12-23 Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO Davies, Thomas Q. Tilby, Michael J. Skolc, David Hall, Adrian Willis, Michael C. Org Lett [Image: see text] Sulfonamides have played a defining role in the history of drug development and continue to be prevalent today. In particular, primary sulfonamides are common in marketed drugs. Here we describe the direct synthesis of these valuable compounds from organometallic reagents and a novel sulfinylamine reagent, t-BuONSO. A variety of (hetero)aryl and alkyl Grignard and organolithium reagents perform well in the reaction, providing primary sulfonamides in good to excellent yields in a convenient one-step process. American Chemical Society 2020-11-25 2020-12-18 /pmc/articles/PMC7754190/ /pubmed/33237777 http://dx.doi.org/10.1021/acs.orglett.0c03505 Text en © 2020 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 | Davies, Thomas Q. Tilby, Michael J. Skolc, David Hall, Adrian Willis, Michael C. Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title | Primary Sulfonamide Synthesis Using the Sulfinylamine
Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title_full | Primary Sulfonamide Synthesis Using the Sulfinylamine
Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title_fullStr | Primary Sulfonamide Synthesis Using the Sulfinylamine
Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title_full_unstemmed | Primary Sulfonamide Synthesis Using the Sulfinylamine
Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title_short | Primary Sulfonamide Synthesis Using the Sulfinylamine
Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO |
title_sort | primary sulfonamide synthesis using the sulfinylamine
reagent n-sulfinyl-o-(tert-butyl)hydroxylamine, t-buonso |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754190/ https://www.ncbi.nlm.nih.gov/pubmed/33237777 http://dx.doi.org/10.1021/acs.orglett.0c03505 |
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