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Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles
Tetrazoles play a prominent role in medicinal chemistry due to their role as carboxylate bioisosteres but have largely been overlooked as C–H functionalisation substrates. We herein report the development of a high-yielding and general procedure for the heterobenzylic C–H functionalisation of 5-alky...
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/PMC8528014/ https://www.ncbi.nlm.nih.gov/pubmed/34777760 http://dx.doi.org/10.1039/d1sc04176b |
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author | Wong, Jeff Y. F. Thomson, Christopher G. Vilela, Filipe Barker, Graeme |
author_facet | Wong, Jeff Y. F. Thomson, Christopher G. Vilela, Filipe Barker, Graeme |
author_sort | Wong, Jeff Y. F. |
collection | PubMed |
description | Tetrazoles play a prominent role in medicinal chemistry due to their role as carboxylate bioisosteres but have largely been overlooked as C–H functionalisation substrates. We herein report the development of a high-yielding and general procedure for the heterobenzylic C–H functionalisation of 5-alkyltetrazoles in up to 97% yield under batch conditions using a metalation/electrophilic trapping strategy. Through the use of thermal imaging to identify potentially unsafe exotherms, a continuous flow procedure using a flash chemistry strategy has also been developed, allowing products to be accessed in up to 95% yield. This enabled an extremely high productivity rate of 141 g h(−1) to be achieved on an entry-level flow system. |
format | Online Article Text |
id | pubmed-8528014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85280142021-11-12 Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles Wong, Jeff Y. F. Thomson, Christopher G. Vilela, Filipe Barker, Graeme Chem Sci Chemistry Tetrazoles play a prominent role in medicinal chemistry due to their role as carboxylate bioisosteres but have largely been overlooked as C–H functionalisation substrates. We herein report the development of a high-yielding and general procedure for the heterobenzylic C–H functionalisation of 5-alkyltetrazoles in up to 97% yield under batch conditions using a metalation/electrophilic trapping strategy. Through the use of thermal imaging to identify potentially unsafe exotherms, a continuous flow procedure using a flash chemistry strategy has also been developed, allowing products to be accessed in up to 95% yield. This enabled an extremely high productivity rate of 141 g h(−1) to be achieved on an entry-level flow system. The Royal Society of Chemistry 2021-09-15 /pmc/articles/PMC8528014/ /pubmed/34777760 http://dx.doi.org/10.1039/d1sc04176b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Wong, Jeff Y. F. Thomson, Christopher G. Vilela, Filipe Barker, Graeme Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title | Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title_full | Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title_fullStr | Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title_full_unstemmed | Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title_short | Flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
title_sort | flash chemistry enables high productivity metalation-substitution of 5-alkyltetrazoles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528014/ https://www.ncbi.nlm.nih.gov/pubmed/34777760 http://dx.doi.org/10.1039/d1sc04176b |
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