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Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives
Quinazolinones are interesting materials because of their valuable biological effects. In this study some new 2,3-disubstituted-4(3H)quinqzolinone derivatives were synthesized from anthranilic acid in six steps by introducing a new chiral center to the aliphatic side chain of the quinazolinone. In t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500554/ https://www.ncbi.nlm.nih.gov/pubmed/23181076 |
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author | Hassanzadeh, F. Khajouei, M. Rahmani Hakimelahi, G.H. Jafari, E. Khodarahmi, G.A. |
author_facet | Hassanzadeh, F. Khajouei, M. Rahmani Hakimelahi, G.H. Jafari, E. Khodarahmi, G.A. |
author_sort | Hassanzadeh, F. |
collection | PubMed |
description | Quinazolinones are interesting materials because of their valuable biological effects. In this study some new 2,3-disubstituted-4(3H)quinqzolinone derivatives were synthesized from anthranilic acid in six steps by introducing a new chiral center to the aliphatic side chain of the quinazolinone. In the last step, a single acylation on the hydrazine moiety afforded final compounds. The structures of compounds were confirmed by IR, (1)HNMR and Mass spectra. |
format | Online Article Text |
id | pubmed-3500554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35005542012-11-23 Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives Hassanzadeh, F. Khajouei, M. Rahmani Hakimelahi, G.H. Jafari, E. Khodarahmi, G.A. Res Pharm Sci Original Article Quinazolinones are interesting materials because of their valuable biological effects. In this study some new 2,3-disubstituted-4(3H)quinqzolinone derivatives were synthesized from anthranilic acid in six steps by introducing a new chiral center to the aliphatic side chain of the quinazolinone. In the last step, a single acylation on the hydrazine moiety afforded final compounds. The structures of compounds were confirmed by IR, (1)HNMR and Mass spectra. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3500554/ /pubmed/23181076 Text en Copyright: © Journal of Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hassanzadeh, F. Khajouei, M. Rahmani Hakimelahi, G.H. Jafari, E. Khodarahmi, G.A. Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title | Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title_full | Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title_fullStr | Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title_full_unstemmed | Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title_short | Synthesis of some new 2,3-disubstituted-4(3H)quinazolinone derivatives |
title_sort | synthesis of some new 2,3-disubstituted-4(3h)quinazolinone derivatives |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500554/ https://www.ncbi.nlm.nih.gov/pubmed/23181076 |
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