4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide

In the title compound, C(14)H(12)ClN(3)OS, the short exocyclic N—C bond lengths indicate resonance in the thiourea part of the mol­ecule. The title compound is stabilized by an intra­molecular N—H⋯N hydrogen bond, which results in the formation of a six-membered ring. In addition, it shows a synperi...

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Detalles Bibliográficos
Autores principales: Binzet, Gün, Emen, Fatih Mehmet, Flörke, Ulrich, Yeşilkaynak, Tuncay, Külcü, Nevzat, Arslan, Hakan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967990/
https://www.ncbi.nlm.nih.gov/pubmed/21581720
http://dx.doi.org/10.1107/S1600536808041123
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author Binzet, Gün
Emen, Fatih Mehmet
Flörke, Ulrich
Yeşilkaynak, Tuncay
Külcü, Nevzat
Arslan, Hakan
author_facet Binzet, Gün
Emen, Fatih Mehmet
Flörke, Ulrich
Yeşilkaynak, Tuncay
Külcü, Nevzat
Arslan, Hakan
author_sort Binzet, Gün
collection PubMed
description In the title compound, C(14)H(12)ClN(3)OS, the short exocyclic N—C bond lengths indicate resonance in the thiourea part of the mol­ecule. The title compound is stabilized by an intra­molecular N—H⋯N hydrogen bond, which results in the formation of a six-membered ring. In addition, it shows a synperiplanar conformation between the thio­carbonyl group and the pyridine group. Inter­molecular N—H⋯S and C—H⋯O inter­actions are also present.
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spelling pubmed-29679902010-12-30 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide Binzet, Gün Emen, Fatih Mehmet Flörke, Ulrich Yeşilkaynak, Tuncay Külcü, Nevzat Arslan, Hakan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(12)ClN(3)OS, the short exocyclic N—C bond lengths indicate resonance in the thiourea part of the mol­ecule. The title compound is stabilized by an intra­molecular N—H⋯N hydrogen bond, which results in the formation of a six-membered ring. In addition, it shows a synperiplanar conformation between the thio­carbonyl group and the pyridine group. Inter­molecular N—H⋯S and C—H⋯O inter­actions are also present. International Union of Crystallography 2008-12-10 /pmc/articles/PMC2967990/ /pubmed/21581720 http://dx.doi.org/10.1107/S1600536808041123 Text en © Binzet 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
Binzet, Gün
Emen, Fatih Mehmet
Flörke, Ulrich
Yeşilkaynak, Tuncay
Külcü, Nevzat
Arslan, Hakan
4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title_full 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title_fullStr 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title_full_unstemmed 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title_short 4-Chloro-N-[N-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
title_sort 4-chloro-n-[n-(6-methyl-2-pyrid­yl)car­bamo­thio­yl]benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967990/
https://www.ncbi.nlm.nih.gov/pubmed/21581720
http://dx.doi.org/10.1107/S1600536808041123
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