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2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile

In the title compound, C(22)H(14)ClN(3), prepared by a one-pot reaction under microwave irradiation, the dihedral angles between the central pyridine ring and the pendant naphthyl and chloro­benzene ring systems are 49.2 (2) and 58.2 (3)°, respectively. In the crystal, inversion dimers linked by pai...

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Autores principales: Wei, Hong-Xia, Zhu, Jing, Li, Ming, Wang, Jian-qiang, Guo, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379409/
https://www.ncbi.nlm.nih.gov/pubmed/22719607
http://dx.doi.org/10.1107/S1600536812020909
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author Wei, Hong-Xia
Zhu, Jing
Li, Ming
Wang, Jian-qiang
Guo, Cheng
author_facet Wei, Hong-Xia
Zhu, Jing
Li, Ming
Wang, Jian-qiang
Guo, Cheng
author_sort Wei, Hong-Xia
collection PubMed
description In the title compound, C(22)H(14)ClN(3), prepared by a one-pot reaction under microwave irradiation, the dihedral angles between the central pyridine ring and the pendant naphthyl and chloro­benzene ring systems are 49.2 (2) and 58.2 (3)°, respectively. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The pyridine N atom is the acceptor.
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spelling pubmed-33794092012-06-20 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile Wei, Hong-Xia Zhu, Jing Li, Ming Wang, Jian-qiang Guo, Cheng Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(14)ClN(3), prepared by a one-pot reaction under microwave irradiation, the dihedral angles between the central pyridine ring and the pendant naphthyl and chloro­benzene ring systems are 49.2 (2) and 58.2 (3)°, respectively. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The pyridine N atom is the acceptor. International Union of Crystallography 2012-05-23 /pmc/articles/PMC3379409/ /pubmed/22719607 http://dx.doi.org/10.1107/S1600536812020909 Text en © Wei et al. 2012 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 Organic Papers
Wei, Hong-Xia
Zhu, Jing
Li, Ming
Wang, Jian-qiang
Guo, Cheng
2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title_full 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title_fullStr 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title_full_unstemmed 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title_short 2-Amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
title_sort 2-amino-4-(2-chloro­phen­yl)-6-(naph­thalen-1-yl)pyridine-3-carbonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379409/
https://www.ncbi.nlm.nih.gov/pubmed/22719607
http://dx.doi.org/10.1107/S1600536812020909
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