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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-...

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Autores principales: Hoffman, Gavin R., Schoffstall, Allen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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