N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide

In the crystal structure of the title compound, C(14)H(15)ClN(2)O(3)S, each mol­ecule is connected via inter­molecular C—H⋯O hydrogen bonds to three further mol­ecules, generating a three-dimensional network. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 40.7 (2)° with the 4-chloro­pyr...

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Detalles Bibliográficos
Autores principales: Bühler, Stefanie, Schollmeyer, Dieter, Albrecht, Wolfgang, Laufer, Stefan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011658/
https://www.ncbi.nlm.nih.gov/pubmed/21589598
http://dx.doi.org/10.1107/S1600536810048336
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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 In the crystal structure of the title compound, C(14)H(15)ClN(2)O(3)S, each mol­ecule is connected via inter­molecular C—H⋯O hydrogen bonds to three further mol­ecules, generating a three-dimensional network. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 40.7 (2)° with the 4-chloro­pyridine ring.
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spelling pubmed-30116582010-12-30 N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide Bühler, Stefanie Schollmeyer, Dieter Albrecht, Wolfgang Laufer, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(14)H(15)ClN(2)O(3)S, each mol­ecule is connected via inter­molecular C—H⋯O hydrogen bonds to three further mol­ecules, generating a three-dimensional network. The 4-methyl­phenyl­sulfonyl ring forms a dihedral angle of 40.7 (2)° with the 4-chloro­pyridine ring. International Union of Crystallography 2010-11-27 /pmc/articles/PMC3011658/ /pubmed/21589598 http://dx.doi.org/10.1107/S1600536810048336 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-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title_full N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title_fullStr N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title_short N-(4-Chloro­pyridin-2-yl)-N-meth­oxy­methyl-4-methyl­benzene­sulfonamide
title_sort n-(4-chloro­pyridin-2-yl)-n-meth­oxy­methyl-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011658/
https://www.ncbi.nlm.nih.gov/pubmed/21589598
http://dx.doi.org/10.1107/S1600536810048336
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AT albrechtwolfgang n4chloropyridin2ylnmethoxymethyl4methylbenzenesulfonamide
AT lauferstefan n4chloropyridin2ylnmethoxymethyl4methylbenzenesulfonamide

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