4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine

The crystal structure of the title compound, C(14)H(11)ClN(2)O(2)S, features a three-dimensional network stabilized by π–π inter­actions between the rings of the 4-methyl­phenyl­sulfonyl protecting group [centroid–centroid distance = 3.623 (1) Å]. The 4-methyl­phenyl­sulfonyl ring makes a dihedral a...

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Detalles Bibliográficos
Autores principales: Selig, Roland, Schollmeyer, Dieter, Albrecht, Wolfgang, 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/PMC2972132/
https://www.ncbi.nlm.nih.gov/pubmed/21578755
http://dx.doi.org/10.1107/S1600536809044559
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author Selig, Roland
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
author_facet Selig, Roland
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
author_sort Selig, Roland
collection PubMed
description The crystal structure of the title compound, C(14)H(11)ClN(2)O(2)S, features a three-dimensional network stabilized by π–π inter­actions between the rings of the 4-methyl­phenyl­sulfonyl protecting group [centroid–centroid distance = 3.623 (1) Å]. The 4-methyl­phenyl­sulfonyl ring makes a dihedral angle of 79.60 (6)° with the 4-chloro-1H-pyrrolo[2,3-b]pyridine unit.
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spelling pubmed-29721322010-12-30 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine Selig, Roland 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(11)ClN(2)O(2)S, features a three-dimensional network stabilized by π–π inter­actions between the rings of the 4-methyl­phenyl­sulfonyl protecting group [centroid–centroid distance = 3.623 (1) Å]. The 4-methyl­phenyl­sulfonyl ring makes a dihedral angle of 79.60 (6)° with the 4-chloro-1H-pyrrolo[2,3-b]pyridine unit. International Union of Crystallography 2009-11-07 /pmc/articles/PMC2972132/ /pubmed/21578755 http://dx.doi.org/10.1107/S1600536809044559 Text en © Selig 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
Selig, Roland
Schollmeyer, Dieter
Albrecht, Wolfgang
Laufer, Stefan
4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title_full 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title_fullStr 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title_full_unstemmed 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title_short 4-Chloro-1-(4-methyl­phenyl­sulfon­yl)-1H-pyrrolo[2,3-b]pyridine
title_sort 4-chloro-1-(4-methyl­phenyl­sulfon­yl)-1h-pyrrolo[2,3-b]pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972132/
https://www.ncbi.nlm.nih.gov/pubmed/21578755
http://dx.doi.org/10.1107/S1600536809044559
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AT lauferstefan 4chloro14methylphenylsulfonyl1hpyrrolo23bpyridine

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