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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...

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Detalles Bibliográficos
Autores principales: Badolato, Mariateresa, Aiello, Francesca, Neamati, Nouri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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.
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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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