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Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst

The title compound, C(14)H(18)N(4)O, synthesized from an unconventional microwave-assisted method using caesium carbonate as catalyst, has an approximately planar conformation with the pyridyl and pyrazole rings inclined by a dihedral angle of 7.94 (3)°, allowing the formation of an intra­molecular...

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Detalles Bibliográficos
Autores principales: Macías, Mario A., Orrego-Hernández, Jessica, Portilla, Jaime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095859/
https://www.ncbi.nlm.nih.gov/pubmed/27840734
http://dx.doi.org/10.1107/S2056989016017187
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author Macías, Mario A.
Orrego-Hernández, Jessica
Portilla, Jaime
author_facet Macías, Mario A.
Orrego-Hernández, Jessica
Portilla, Jaime
author_sort Macías, Mario A.
collection PubMed
description The title compound, C(14)H(18)N(4)O, synthesized from an unconventional microwave-assisted method using caesium carbonate as catalyst, has an approximately planar conformation with the pyridyl and pyrazole rings inclined by a dihedral angle of 7.94 (3)°, allowing the formation of an intra­molecular N—H⋯N hydrogen bond. The supra­molecular assembly has a three-dimensional arrangement controlled mainly by weak C—H⋯O and C—H⋯π inter­actions.
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spelling pubmed-50958592016-11-11 Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst Macías, Mario A. Orrego-Hernández, Jessica Portilla, Jaime Acta Crystallogr E Crystallogr Commun Research Communications The title compound, C(14)H(18)N(4)O, synthesized from an unconventional microwave-assisted method using caesium carbonate as catalyst, has an approximately planar conformation with the pyridyl and pyrazole rings inclined by a dihedral angle of 7.94 (3)°, allowing the formation of an intra­molecular N—H⋯N hydrogen bond. The supra­molecular assembly has a three-dimensional arrangement controlled mainly by weak C—H⋯O and C—H⋯π inter­actions. International Union of Crystallography 2016-10-28 /pmc/articles/PMC5095859/ /pubmed/27840734 http://dx.doi.org/10.1107/S2056989016017187 Text en © Macías et al. 2016 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Communications
Macías, Mario A.
Orrego-Hernández, Jessica
Portilla, Jaime
Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title_full Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title_fullStr Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title_full_unstemmed Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title_short Crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
title_sort crystal structure of 5-butyl­amino-3-methyl-1-(pyridin-2-yl)-1h-pyrazole-4-carbaldehyde obtained from a microwave-assisted reaction using caesium carbonate as catalyst
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095859/
https://www.ncbi.nlm.nih.gov/pubmed/27840734
http://dx.doi.org/10.1107/S2056989016017187
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