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N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide

The crystal structure of the title compound, C(14)H(13)ClN(2)O(3)S, features a three-dimensional network stabilized by inter­molecular C—H⋯O hydrogen bonds between the mol­ecules. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 30.6 (1)° with the 4-chloro­pyridine ring.

Detalles Bibliográficos
Autores principales: Bühler, Stefanie, Schollmeyer, Dieter, Albrecht, Wolfgang, Laufer, Stefan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011710/
https://www.ncbi.nlm.nih.gov/pubmed/21589597
http://dx.doi.org/10.1107/S1600536810048324
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author Bühler, Stefanie
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
author_facet Bühler, Stefanie
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
author_sort Bühler, Stefanie
collection PubMed
description The crystal structure of the title compound, C(14)H(13)ClN(2)O(3)S, features a three-dimensional network stabilized by inter­molecular C—H⋯O hydrogen bonds between the mol­ecules. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 30.6 (1)° with the 4-chloro­pyridine ring.
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spelling pubmed-30117102010-12-30 N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide Bühler, Stefanie Schollmeyer, Dieter Albrecht, Wolfgang Laufer, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(14)H(13)ClN(2)O(3)S, features a three-dimensional network stabilized by inter­molecular C—H⋯O hydrogen bonds between the mol­ecules. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 30.6 (1)° with the 4-chloro­pyridine ring. International Union of Crystallography 2010-11-27 /pmc/articles/PMC3011710/ /pubmed/21589597 http://dx.doi.org/10.1107/S1600536810048324 Text en © Bühler et al. 2010 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
Bühler, Stefanie
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_full N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_fullStr N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_full_unstemmed N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_short N-(4-Chloro­pyridin-2-yl)-N-(4-methyl­phenyl­sulfon­yl)acetamide
title_sort n-(4-chloro­pyridin-2-yl)-n-(4-methyl­phenyl­sulfon­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011710/
https://www.ncbi.nlm.nih.gov/pubmed/21589597
http://dx.doi.org/10.1107/S1600536810048324
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AT lauferstefan n4chloropyridin2yln4methylphenylsulfonylacetamide