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N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide
In the title compound, C(14)H(20)N(2)O(2)S, the sulfonamide O atoms lie to one side of the benzene ring and the aminobicycloheptanyl to the other side [C(ar)—S—N—C torsion angle = −57.93 (11)°; ar = aromatic]. An intramolecular N—H⋯N hydrogen bond is formed. In the crystal, a supramolecular cha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393301/ https://www.ncbi.nlm.nih.gov/pubmed/22807858 http://dx.doi.org/10.1107/S1600536812025421 |
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author | Abdel-Aziz, Alaa A.-M. El-Azab, Adel S. El-Sherbeny, Magda A. Ng, Seik Weng Tiekink, Edward R. T. |
author_facet | Abdel-Aziz, Alaa A.-M. El-Azab, Adel S. El-Sherbeny, Magda A. Ng, Seik Weng Tiekink, Edward R. T. |
author_sort | Abdel-Aziz, Alaa A.-M. |
collection | PubMed |
description | In the title compound, C(14)H(20)N(2)O(2)S, the sulfonamide O atoms lie to one side of the benzene ring and the aminobicycloheptanyl to the other side [C(ar)—S—N—C torsion angle = −57.93 (11)°; ar = aromatic]. An intramolecular N—H⋯N hydrogen bond is formed. In the crystal, a supramolecular chain is formed along the b axis via N—H⋯O and N—H⋯N hydrogen bonds. |
format | Online Article Text |
id | pubmed-3393301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33933012012-07-17 N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide Abdel-Aziz, Alaa A.-M. El-Azab, Adel S. El-Sherbeny, Magda A. Ng, Seik Weng Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(20)N(2)O(2)S, the sulfonamide O atoms lie to one side of the benzene ring and the aminobicycloheptanyl to the other side [C(ar)—S—N—C torsion angle = −57.93 (11)°; ar = aromatic]. An intramolecular N—H⋯N hydrogen bond is formed. In the crystal, a supramolecular chain is formed along the b axis via N—H⋯O and N—H⋯N hydrogen bonds. International Union of Crystallography 2012-06-13 /pmc/articles/PMC3393301/ /pubmed/22807858 http://dx.doi.org/10.1107/S1600536812025421 Text en © Abdel-Aziz et al. 2012 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 Abdel-Aziz, Alaa A.-M. El-Azab, Adel S. El-Sherbeny, Magda A. Ng, Seik Weng Tiekink, Edward R. T. N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title |
N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title_full |
N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title_fullStr |
N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title_full_unstemmed |
N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title_short |
N-(3-Aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
title_sort | n-(3-aminobicyclo[2.2.1]heptan-2-yl)-4-methylbenzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393301/ https://www.ncbi.nlm.nih.gov/pubmed/22807858 http://dx.doi.org/10.1107/S1600536812025421 |
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