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2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design
2,3-Dihydroquinazolin-4-one (DHQ) belongs to the class of nitrogen-containing heterocyclic compounds representing a core structural component in various biologically active compounds. In the past decades, several methodologies have been developed for the synthesis of the DHQ framework, especially th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080947/ https://www.ncbi.nlm.nih.gov/pubmed/35542353 http://dx.doi.org/10.1039/c8ra02827c |
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author | Badolato, Mariateresa Aiello, Francesca Neamati, Nouri |
author_facet | Badolato, Mariateresa Aiello, Francesca Neamati, Nouri |
author_sort | Badolato, Mariateresa |
collection | PubMed |
description | 2,3-Dihydroquinazolin-4-one (DHQ) belongs to the class of nitrogen-containing heterocyclic compounds representing a core structural component in various biologically active compounds. In the past decades, several methodologies have been developed for the synthesis of the DHQ framework, especially the 2-substituted derivatives. Unfortunately, multistep syntheses, harsh reaction conditions, and the use of toxic reagents and solvents have limited their full potential as a versatile fragment. Recently, use of green chemistry and alternative strategies are being explored to prepare diverse DHQ derivatives. This fragment is used as a synthon for the preparation of biologically active quinazolinones and as a functional substrate for the synthesis of modified DHQ derivatives exhibiting different biological properties. In this review, we provide a comprehensive assessment of the synthesis and biological evaluations of DHQ derivatives. |
format | Online Article Text |
id | pubmed-9080947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90809472022-05-09 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design Badolato, Mariateresa Aiello, Francesca Neamati, Nouri RSC Adv Chemistry 2,3-Dihydroquinazolin-4-one (DHQ) belongs to the class of nitrogen-containing heterocyclic compounds representing a core structural component in various biologically active compounds. In the past decades, several methodologies have been developed for the synthesis of the DHQ framework, especially the 2-substituted derivatives. Unfortunately, multistep syntheses, harsh reaction conditions, and the use of toxic reagents and solvents have limited their full potential as a versatile fragment. Recently, use of green chemistry and alternative strategies are being explored to prepare diverse DHQ derivatives. This fragment is used as a synthon for the preparation of biologically active quinazolinones and as a functional substrate for the synthesis of modified DHQ derivatives exhibiting different biological properties. In this review, we provide a comprehensive assessment of the synthesis and biological evaluations of DHQ derivatives. The Royal Society of Chemistry 2018-06-07 /pmc/articles/PMC9080947/ /pubmed/35542353 http://dx.doi.org/10.1039/c8ra02827c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Badolato, Mariateresa Aiello, Francesca Neamati, Nouri 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title | 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title_full | 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title_fullStr | 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title_full_unstemmed | 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title_short | 2,3-Dihydroquinazolin-4(1H)-one as a privileged scaffold in drug design |
title_sort | 2,3-dihydroquinazolin-4(1h)-one as a privileged scaffold in drug design |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080947/ https://www.ncbi.nlm.nih.gov/pubmed/35542353 http://dx.doi.org/10.1039/c8ra02827c |
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