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An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry
A straightforward, mild and cost-efficient synthesis of various arylamides in water was accomplished using versatile benzotriazole chemistry. Acylation of various amines was achieved in water at room temperature as well as under microwave irradiation. The developed protocol unfolds the synthesis of...
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/PMC7321353/ https://www.ncbi.nlm.nih.gov/pubmed/32481504 http://dx.doi.org/10.3390/molecules25112501 |
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author | Ibrahim, Tarek S. Seliem, Israa A. Panda, Siva S. Al-Mahmoudy, Amany M. M. Abdel-Samii, Zakaria K. M. Alhakamy, Nabil A. Asfour, Hani Z. Elagawany, Mohamed |
author_facet | Ibrahim, Tarek S. Seliem, Israa A. Panda, Siva S. Al-Mahmoudy, Amany M. M. Abdel-Samii, Zakaria K. M. Alhakamy, Nabil A. Asfour, Hani Z. Elagawany, Mohamed |
author_sort | Ibrahim, Tarek S. |
collection | PubMed |
description | A straightforward, mild and cost-efficient synthesis of various arylamides in water was accomplished using versatile benzotriazole chemistry. Acylation of various amines was achieved in water at room temperature as well as under microwave irradiation. The developed protocol unfolds the synthesis of amino acid aryl amides, drug conjugates and benzimidazoles. The environmentally friendly synthesis, short reaction time, simple workup, high yields, mild conditions and free of racemization are the key advantages of this protocol. |
format | Online Article Text |
id | pubmed-7321353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73213532020-06-29 An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry Ibrahim, Tarek S. Seliem, Israa A. Panda, Siva S. Al-Mahmoudy, Amany M. M. Abdel-Samii, Zakaria K. M. Alhakamy, Nabil A. Asfour, Hani Z. Elagawany, Mohamed Molecules Article A straightforward, mild and cost-efficient synthesis of various arylamides in water was accomplished using versatile benzotriazole chemistry. Acylation of various amines was achieved in water at room temperature as well as under microwave irradiation. The developed protocol unfolds the synthesis of amino acid aryl amides, drug conjugates and benzimidazoles. The environmentally friendly synthesis, short reaction time, simple workup, high yields, mild conditions and free of racemization are the key advantages of this protocol. MDPI 2020-05-28 /pmc/articles/PMC7321353/ /pubmed/32481504 http://dx.doi.org/10.3390/molecules25112501 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 Ibrahim, Tarek S. Seliem, Israa A. Panda, Siva S. Al-Mahmoudy, Amany M. M. Abdel-Samii, Zakaria K. M. Alhakamy, Nabil A. Asfour, Hani Z. Elagawany, Mohamed An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title | An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title_full | An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title_fullStr | An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title_full_unstemmed | An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title_short | An Efficient Greener Approach for N-acylation of Amines in Water Using Benzotriazole Chemistry |
title_sort | efficient greener approach for n-acylation of amines in water using benzotriazole chemistry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321353/ https://www.ncbi.nlm.nih.gov/pubmed/32481504 http://dx.doi.org/10.3390/molecules25112501 |
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