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Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature
A Cu(ii)-catalyzed, effective C–N coupling of 2-aminobenzothiazoles with boronic acids in acetonitrile under open vessel chemistry was achieved. This protocol demonstrates the N-arylation of 2-aminobenzothiazoles with a broad range of differently substituted phenylboronic acids at room temperature a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248544/ https://www.ncbi.nlm.nih.gov/pubmed/37304782 http://dx.doi.org/10.1039/d3ra02979d |
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author | Radhika, Sankaran Chandravarkar, Aravind Anilkumar, Gopinathan |
author_facet | Radhika, Sankaran Chandravarkar, Aravind Anilkumar, Gopinathan |
author_sort | Radhika, Sankaran |
collection | PubMed |
description | A Cu(ii)-catalyzed, effective C–N coupling of 2-aminobenzothiazoles with boronic acids in acetonitrile under open vessel chemistry was achieved. This protocol demonstrates the N-arylation of 2-aminobenzothiazoles with a broad range of differently substituted phenylboronic acids at room temperature and accomplishes moderate to excellent yields of the desired products. Under the optimized condition, phenylboronic acids bearing halogen at the para and meta positions were found to be more fruitful. |
format | Online Article Text |
id | pubmed-10248544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-102485442023-06-09 Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature Radhika, Sankaran Chandravarkar, Aravind Anilkumar, Gopinathan RSC Adv Chemistry A Cu(ii)-catalyzed, effective C–N coupling of 2-aminobenzothiazoles with boronic acids in acetonitrile under open vessel chemistry was achieved. This protocol demonstrates the N-arylation of 2-aminobenzothiazoles with a broad range of differently substituted phenylboronic acids at room temperature and accomplishes moderate to excellent yields of the desired products. Under the optimized condition, phenylboronic acids bearing halogen at the para and meta positions were found to be more fruitful. The Royal Society of Chemistry 2023-06-08 /pmc/articles/PMC10248544/ /pubmed/37304782 http://dx.doi.org/10.1039/d3ra02979d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Radhika, Sankaran Chandravarkar, Aravind Anilkumar, Gopinathan Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title | Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title_full | Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title_fullStr | Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title_full_unstemmed | Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title_short | Cu(ii)-catalyzed C–N coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
title_sort | cu(ii)-catalyzed c–n coupling of 2-aminobenzothiazoles with boronic acids at room temperature |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248544/ https://www.ncbi.nlm.nih.gov/pubmed/37304782 http://dx.doi.org/10.1039/d3ra02979d |
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