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N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN]
The crystal structure of the title compound, C(21)H(22)N(2)O(2)S, shows a network of N—H⋯N and N—H⋯O hydrogen bonds. The tolyl and 1-phenyl rings are almost mutually coplanar [7.89 (9)°], while the 2-phenyl ring makes a dihedral angle of 50.8 (1) ° with the 1-phenyl ring. An intramolecular N—H⋯N hy...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011471/ https://www.ncbi.nlm.nih.gov/pubmed/21589615 http://dx.doi.org/10.1107/S1600536810049159 |
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author | Schlemmer, Claudine Schollmeyer, Dieter Blank, Nancy Stoye, Alexander Opatz, Till |
author_facet | Schlemmer, Claudine Schollmeyer, Dieter Blank, Nancy Stoye, Alexander Opatz, Till |
author_sort | Schlemmer, Claudine |
collection | PubMed |
description | The crystal structure of the title compound, C(21)H(22)N(2)O(2)S, shows a network of N—H⋯N and N—H⋯O hydrogen bonds. The tolyl and 1-phenyl rings are almost mutually coplanar [7.89 (9)°], while the 2-phenyl ring makes a dihedral angle of 50.8 (1) ° with the 1-phenyl ring. An intramolecular N—H⋯N hydrogen bond stabilizes the molecular conformation. |
format | Text |
id | pubmed-3011471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30114712010-12-30 N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] Schlemmer, Claudine Schollmeyer, Dieter Blank, Nancy Stoye, Alexander Opatz, Till Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(21)H(22)N(2)O(2)S, shows a network of N—H⋯N and N—H⋯O hydrogen bonds. The tolyl and 1-phenyl rings are almost mutually coplanar [7.89 (9)°], while the 2-phenyl ring makes a dihedral angle of 50.8 (1) ° with the 1-phenyl ring. An intramolecular N—H⋯N hydrogen bond stabilizes the molecular conformation. International Union of Crystallography 2010-11-27 /pmc/articles/PMC3011471/ /pubmed/21589615 http://dx.doi.org/10.1107/S1600536810049159 Text en © Schlemmer 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 Schlemmer, Claudine Schollmeyer, Dieter Blank, Nancy Stoye, Alexander Opatz, Till N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title |
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title_full |
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title_fullStr |
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title_full_unstemmed |
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title_short |
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(S,S)-TsDPEN] |
title_sort | n-[(1s,2s)-2-amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide [(s,s)-tsdpen] |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011471/ https://www.ncbi.nlm.nih.gov/pubmed/21589615 http://dx.doi.org/10.1107/S1600536810049159 |
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