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Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines
Pyrazines and pyridazines fused to 1,2,3-triazoles comprise a set of heterocycles obtained through a variety of synthetic routes. Two typical modes of constructing these heterocyclic ring systems are cyclizing a heterocyclic diamine with a nitrite or reacting hydrazine hydrate with dicarbonyl 1,2,3-...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329905/ https://www.ncbi.nlm.nih.gov/pubmed/35897857 http://dx.doi.org/10.3390/molecules27154681 |
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author | Hoffman, Gavin R. Schoffstall, Allen M. |
author_facet | Hoffman, Gavin R. Schoffstall, Allen M. |
author_sort | Hoffman, Gavin R. |
collection | PubMed |
description | Pyrazines and pyridazines fused to 1,2,3-triazoles comprise a set of heterocycles obtained through a variety of synthetic routes. Two typical modes of constructing these heterocyclic ring systems are cyclizing a heterocyclic diamine with a nitrite or reacting hydrazine hydrate with dicarbonyl 1,2,3-triazoles. Several unique methods are known, particularly for the synthesis of 1,2,3-triazolo[1,5-a]pyrazines and their benzo-fused quinoxaline and quinoxalinone-containing analogs. Recent applications detail the use of these heterocycles in medicinal chemistry (c-Met inhibition or GABA(A) modulating activity) as fluorescent probes and as structural units of polymers. |
format | Online Article Text |
id | pubmed-9329905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93299052022-07-29 Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines Hoffman, Gavin R. Schoffstall, Allen M. Molecules Review Pyrazines and pyridazines fused to 1,2,3-triazoles comprise a set of heterocycles obtained through a variety of synthetic routes. Two typical modes of constructing these heterocyclic ring systems are cyclizing a heterocyclic diamine with a nitrite or reacting hydrazine hydrate with dicarbonyl 1,2,3-triazoles. Several unique methods are known, particularly for the synthesis of 1,2,3-triazolo[1,5-a]pyrazines and their benzo-fused quinoxaline and quinoxalinone-containing analogs. Recent applications detail the use of these heterocycles in medicinal chemistry (c-Met inhibition or GABA(A) modulating activity) as fluorescent probes and as structural units of polymers. MDPI 2022-07-22 /pmc/articles/PMC9329905/ /pubmed/35897857 http://dx.doi.org/10.3390/molecules27154681 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hoffman, Gavin R. Schoffstall, Allen M. Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title | Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title_full | Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title_fullStr | Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title_full_unstemmed | Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title_short | Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines |
title_sort | syntheses and applications of 1,2,3-triazole-fused pyrazines and pyridazines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329905/ https://www.ncbi.nlm.nih.gov/pubmed/35897857 http://dx.doi.org/10.3390/molecules27154681 |
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