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Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles
A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C–N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221555/ https://www.ncbi.nlm.nih.gov/pubmed/32295143 http://dx.doi.org/10.3390/molecules25081788 |
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author | Boddapati, S. N. Murthy Tamminana, Ramana Gollapudi, Ravi Kumar Nurbasha, Sharmila Assal, Mohamed E. Alduhaish, Osamah Siddiqui, Mohammed Rafiq H. Bollikolla, Hari Babu Adil, Syed Farooq |
author_facet | Boddapati, S. N. Murthy Tamminana, Ramana Gollapudi, Ravi Kumar Nurbasha, Sharmila Assal, Mohamed E. Alduhaish, Osamah Siddiqui, Mohammed Rafiq H. Bollikolla, Hari Babu Adil, Syed Farooq |
author_sort | Boddapati, S. N. Murthy |
collection | PubMed |
description | A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C–N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C–N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products. |
format | Online Article Text |
id | pubmed-7221555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72215552020-05-22 Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles Boddapati, S. N. Murthy Tamminana, Ramana Gollapudi, Ravi Kumar Nurbasha, Sharmila Assal, Mohamed E. Alduhaish, Osamah Siddiqui, Mohammed Rafiq H. Bollikolla, Hari Babu Adil, Syed Farooq Molecules Article A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C–N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C–N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products. MDPI 2020-04-14 /pmc/articles/PMC7221555/ /pubmed/32295143 http://dx.doi.org/10.3390/molecules25081788 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Boddapati, S. N. Murthy Tamminana, Ramana Gollapudi, Ravi Kumar Nurbasha, Sharmila Assal, Mohamed E. Alduhaish, Osamah Siddiqui, Mohammed Rafiq H. Bollikolla, Hari Babu Adil, Syed Farooq Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title | Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title_full | Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title_fullStr | Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title_full_unstemmed | Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title_short | Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles |
title_sort | copper-promoted one-pot approach: synthesis of benzimidazoles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221555/ https://www.ncbi.nlm.nih.gov/pubmed/32295143 http://dx.doi.org/10.3390/molecules25081788 |
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