Cargando…

N-Benzyl­pyridine-2-sulfonamide

The title compound, C(12)H(12)N(2)O(2)S, was obtained by the reaction of 2-mercaptopyridine and benzyl­amine. The dihedral angle between the benzene and pyridine rings is 75.75 (9)°. In the crystal, mol­ecules are linked into chains along the c axis by N—H⋯O and N—H⋯N hydrogen bonds; the chains are...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Xiao-Ping, Han, Shou-Fa
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969775/
https://www.ncbi.nlm.nih.gov/pubmed/21583257
http://dx.doi.org/10.1107/S1600536809018054
_version_ 1782190256369434624
author Chen, Xiao-Ping
Han, Shou-Fa
author_facet Chen, Xiao-Ping
Han, Shou-Fa
author_sort Chen, Xiao-Ping
collection PubMed
description The title compound, C(12)H(12)N(2)O(2)S, was obtained by the reaction of 2-mercaptopyridine and benzyl­amine. The dihedral angle between the benzene and pyridine rings is 75.75 (9)°. In the crystal, mol­ecules are linked into chains along the c axis by N—H⋯O and N—H⋯N hydrogen bonds; the chains are cross-linked into a two-dimensional network parallel to the bc plane via C—H⋯O hydrogen bonds.
format Text
id pubmed-2969775
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29697752010-12-30 N-Benzyl­pyridine-2-sulfonamide Chen, Xiao-Ping Han, Shou-Fa Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(12)N(2)O(2)S, was obtained by the reaction of 2-mercaptopyridine and benzyl­amine. The dihedral angle between the benzene and pyridine rings is 75.75 (9)°. In the crystal, mol­ecules are linked into chains along the c axis by N—H⋯O and N—H⋯N hydrogen bonds; the chains are cross-linked into a two-dimensional network parallel to the bc plane via C—H⋯O hydrogen bonds. International Union of Crystallography 2009-05-29 /pmc/articles/PMC2969775/ /pubmed/21583257 http://dx.doi.org/10.1107/S1600536809018054 Text en © Chen and Han 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
Chen, Xiao-Ping
Han, Shou-Fa
N-Benzyl­pyridine-2-sulfonamide
title N-Benzyl­pyridine-2-sulfonamide
title_full N-Benzyl­pyridine-2-sulfonamide
title_fullStr N-Benzyl­pyridine-2-sulfonamide
title_full_unstemmed N-Benzyl­pyridine-2-sulfonamide
title_short N-Benzyl­pyridine-2-sulfonamide
title_sort n-benzyl­pyridine-2-sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969775/
https://www.ncbi.nlm.nih.gov/pubmed/21583257
http://dx.doi.org/10.1107/S1600536809018054
work_keys_str_mv AT chenxiaoping nbenzylpyridine2sulfonamide
AT hanshoufa nbenzylpyridine2sulfonamide