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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...

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Autores principales: Davies, Thomas Q., Tilby, Michael J., Skolc, David, Hall, Adrian, Willis, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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