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Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines
This paper reports the synthesis of phenyl-substituted 2-alkoxy(methylsulfanyl)-1,2,4-triazolo[1,5-a]quinazolines starting from N-cyanoimidocarbonates and substituted hydrazinobenzoic acids as building blocks. Thionation or chlorination of the inherent lactam moiety in the target compounds followed...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259257/ http://dx.doi.org/10.3390/molecules15107016 |
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author | Al-Salahi, Rashad A. |
author_facet | Al-Salahi, Rashad A. |
author_sort | Al-Salahi, Rashad A. |
collection | PubMed |
description | This paper reports the synthesis of phenyl-substituted 2-alkoxy(methylsulfanyl)-1,2,4-triazolo[1,5-a]quinazolines starting from N-cyanoimidocarbonates and substituted hydrazinobenzoic acids as building blocks. Thionation or chlorination of the inherent lactam moiety in the target compounds followed by treatment with multifunctional nucleophiles provided access to a variety of derivatives. |
format | Online Article Text |
id | pubmed-6259257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62592572018-12-06 Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines Al-Salahi, Rashad A. Molecules Article This paper reports the synthesis of phenyl-substituted 2-alkoxy(methylsulfanyl)-1,2,4-triazolo[1,5-a]quinazolines starting from N-cyanoimidocarbonates and substituted hydrazinobenzoic acids as building blocks. Thionation or chlorination of the inherent lactam moiety in the target compounds followed by treatment with multifunctional nucleophiles provided access to a variety of derivatives. MDPI 2010-10-12 /pmc/articles/PMC6259257/ http://dx.doi.org/10.3390/molecules15107016 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Al-Salahi, Rashad A. Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title | Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title_full | Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title_fullStr | Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title_full_unstemmed | Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title_short | Synthesis and Reactivity of [1,2,4]Triazolo-annelated Quinazolines |
title_sort | synthesis and reactivity of [1,2,4]triazolo-annelated quinazolines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259257/ http://dx.doi.org/10.3390/molecules15107016 |
work_keys_str_mv | AT alsalahirashada synthesisandreactivityof124triazoloannelatedquinazolines |