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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3379409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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