4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine

In the title compound, C(14)H(10)FN(3), the imidazole ring makes dihedral angles of 28.2 (1) and 36.60 (9)° with the pyridine ring and the 4-fluoro­phenyl ring, respectively. The pyridine ring forms a dihedral angle of 44.68 (9)° with the 4-fluoro­phenyl ring. Inter­molecular N—H⋯N hydrogen bonds ar...

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Detalles Bibliográficos
Autores principales: Koch, Pierre, Schollmeyer, Dieter, Laufer, Stefan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968498/
https://www.ncbi.nlm.nih.gov/pubmed/21582228
http://dx.doi.org/10.1107/S1600536809005650
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author Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_facet Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_sort Koch, Pierre
collection PubMed
description In the title compound, C(14)H(10)FN(3), the imidazole ring makes dihedral angles of 28.2 (1) and 36.60 (9)° with the pyridine ring and the 4-fluoro­phenyl ring, respectively. The pyridine ring forms a dihedral angle of 44.68 (9)° with the 4-fluoro­phenyl ring. Inter­molecular N—H⋯N hydrogen bonds are observed in the crystal structure.
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spelling pubmed-29684982010-12-30 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine Koch, Pierre Schollmeyer, Dieter Laufer, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(10)FN(3), the imidazole ring makes dihedral angles of 28.2 (1) and 36.60 (9)° with the pyridine ring and the 4-fluoro­phenyl ring, respectively. The pyridine ring forms a dihedral angle of 44.68 (9)° with the 4-fluoro­phenyl ring. Inter­molecular N—H⋯N hydrogen bonds are observed in the crystal structure. International Union of Crystallography 2009-02-21 /pmc/articles/PMC2968498/ /pubmed/21582228 http://dx.doi.org/10.1107/S1600536809005650 Text en © Koch et al. 2009 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
Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title_full 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title_fullStr 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title_full_unstemmed 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title_short 4-[5-(4-Fluoro­phen­yl)-1H-imidazol-4-yl]pyridine
title_sort 4-[5-(4-fluoro­phen­yl)-1h-imidazol-4-yl]pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968498/
https://www.ncbi.nlm.nih.gov/pubmed/21582228
http://dx.doi.org/10.1107/S1600536809005650
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AT schollmeyerdieter 454fluorophenyl1himidazol4ylpyridine
AT lauferstefan 454fluorophenyl1himidazol4ylpyridine

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