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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...

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Autores principales: Radhika, Sankaran, Chandravarkar, Aravind, Anilkumar, Gopinathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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