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An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines

A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective s...

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Autores principales: Gamonal Ruiz-Crespo, Arturo, Galán-Fernández, Laura, Martínez-Martín, Paloma, Rodríguez-Ubis, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911976/
https://www.ncbi.nlm.nih.gov/pubmed/35268847
http://dx.doi.org/10.3390/molecules27051746
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author Gamonal Ruiz-Crespo, Arturo
Galán-Fernández, Laura
Martínez-Martín, Paloma
Rodríguez-Ubis, Juan Carlos
author_facet Gamonal Ruiz-Crespo, Arturo
Galán-Fernández, Laura
Martínez-Martín, Paloma
Rodríguez-Ubis, Juan Carlos
author_sort Gamonal Ruiz-Crespo, Arturo
collection PubMed
description A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective stepwise substitution, and the bromine atom provides easy access to additional functionalities through both Suzuki and Sonogashira Pd(0) cross-coupling reactions. These synthons represent optimal structures as building blocks in complexation and metalloorganic structures for the tuning of their chelating and photophysical properties.
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spelling pubmed-89119762022-03-11 An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines Gamonal Ruiz-Crespo, Arturo Galán-Fernández, Laura Martínez-Martín, Paloma Rodríguez-Ubis, Juan Carlos Molecules Article A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective stepwise substitution, and the bromine atom provides easy access to additional functionalities through both Suzuki and Sonogashira Pd(0) cross-coupling reactions. These synthons represent optimal structures as building blocks in complexation and metalloorganic structures for the tuning of their chelating and photophysical properties. MDPI 2022-03-07 /pmc/articles/PMC8911976/ /pubmed/35268847 http://dx.doi.org/10.3390/molecules27051746 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 Article
Gamonal Ruiz-Crespo, Arturo
Galán-Fernández, Laura
Martínez-Martín, Paloma
Rodríguez-Ubis, Juan Carlos
An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title_full An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title_fullStr An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title_full_unstemmed An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title_short An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
title_sort orthogonal synthetic approach to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911976/
https://www.ncbi.nlm.nih.gov/pubmed/35268847
http://dx.doi.org/10.3390/molecules27051746
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