Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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
_version_ 1783551445264498688
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
work_keys_str_mv AT ibrahimtareks anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT seliemisraaa anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT pandasivas anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT almahmoudyamanymm anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT abdelsamiizakariakm anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT alhakamynabila anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT asfourhaniz anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT elagawanymohamed anefficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT ibrahimtareks efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT seliemisraaa efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT pandasivas efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT almahmoudyamanymm efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT abdelsamiizakariakm efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT alhakamynabila efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT asfourhaniz efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry
AT elagawanymohamed efficientgreenerapproachfornacylationofaminesinwaterusingbenzotriazolechemistry