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Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst

A simple and versatile method for the synthesis of 1,5-benzodiazepines is via condensation of o-phenylenediamines (OPDA) and ketones in the presence of catalytic amount of H-MCM-22 using acetonitrile as solvent at room temperature. In all the cases, the reactions are highly selective and are complet...

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Detalles Bibliográficos
Autores principales: Majid, Sheikh Abdul, Khanday, Waheed Ahmad, Tomar, Radha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336253/
https://www.ncbi.nlm.nih.gov/pubmed/22570531
http://dx.doi.org/10.1155/2012/510650
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author Majid, Sheikh Abdul
Khanday, Waheed Ahmad
Tomar, Radha
author_facet Majid, Sheikh Abdul
Khanday, Waheed Ahmad
Tomar, Radha
author_sort Majid, Sheikh Abdul
collection PubMed
description A simple and versatile method for the synthesis of 1,5-benzodiazepines is via condensation of o-phenylenediamines (OPDA) and ketones in the presence of catalytic amount of H-MCM-22 using acetonitrile as solvent at room temperature. In all the cases, the reactions are highly selective and are completed within 1–3 h. The method is applicable to both cyclic and acyclic ketones without significant differences. The reaction proceeds efficiently under ambient conditions with good-to-excellent yields.
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spelling pubmed-33362532012-05-08 Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst Majid, Sheikh Abdul Khanday, Waheed Ahmad Tomar, Radha J Biomed Biotechnol Research Article A simple and versatile method for the synthesis of 1,5-benzodiazepines is via condensation of o-phenylenediamines (OPDA) and ketones in the presence of catalytic amount of H-MCM-22 using acetonitrile as solvent at room temperature. In all the cases, the reactions are highly selective and are completed within 1–3 h. The method is applicable to both cyclic and acyclic ketones without significant differences. The reaction proceeds efficiently under ambient conditions with good-to-excellent yields. Hindawi Publishing Corporation 2012 2012-04-11 /pmc/articles/PMC3336253/ /pubmed/22570531 http://dx.doi.org/10.1155/2012/510650 Text en Copyright © 2012 Sheikh Abdul Majid et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Majid, Sheikh Abdul
Khanday, Waheed Ahmad
Tomar, Radha
Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title_full Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title_fullStr Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title_full_unstemmed Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title_short Synthesis of 1,5-Benzodiazepine and Its Derivatives by Condensation Reaction Using H-MCM-22 as Catalyst
title_sort synthesis of 1,5-benzodiazepine and its derivatives by condensation reaction using h-mcm-22 as catalyst
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336253/
https://www.ncbi.nlm.nih.gov/pubmed/22570531
http://dx.doi.org/10.1155/2012/510650
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