1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide

The title compound, C(9)H(12)N(2)O(2)S, is a useful precursor of a variety of modified sulfonamide mol­ecules. Due to the importance of these mol­ecules in biological systems (antibacterials, antidepressants and many other applications), there is a growing inter­est in the discovery of new biologica...

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Detalles Bibliográficos
Autores principales: Bouasla, Radia, Berredjem, Malika, Aouf, Nour-Eddine, Barbey, Carole
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960235/
https://www.ncbi.nlm.nih.gov/pubmed/21201459
http://dx.doi.org/10.1107/S1600536807068158
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author Bouasla, Radia
Berredjem, Malika
Aouf, Nour-Eddine
Barbey, Carole
author_facet Bouasla, Radia
Berredjem, Malika
Aouf, Nour-Eddine
Barbey, Carole
author_sort Bouasla, Radia
collection PubMed
description The title compound, C(9)H(12)N(2)O(2)S, is a useful precursor of a variety of modified sulfonamide mol­ecules. Due to the importance of these mol­ecules in biological systems (antibacterials, antidepressants and many other applications), there is a growing inter­est in the discovery of new biologically active compounds. In the title compound, the mol­ecules are linked by N—H⋯O inter­molecular hydrogen bonds involving the sulfonamide function to form an infinite two-dimensional network parallel to the (001) plane.
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spelling pubmed-29602352010-12-30 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide Bouasla, Radia Berredjem, Malika Aouf, Nour-Eddine Barbey, Carole Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(9)H(12)N(2)O(2)S, is a useful precursor of a variety of modified sulfonamide mol­ecules. Due to the importance of these mol­ecules in biological systems (antibacterials, antidepressants and many other applications), there is a growing inter­est in the discovery of new biologically active compounds. In the title compound, the mol­ecules are linked by N—H⋯O inter­molecular hydrogen bonds involving the sulfonamide function to form an infinite two-dimensional network parallel to the (001) plane. International Union of Crystallography 2008-01-11 /pmc/articles/PMC2960235/ /pubmed/21201459 http://dx.doi.org/10.1107/S1600536807068158 Text en © Bouasla et al. 2008 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
Bouasla, Radia
Berredjem, Malika
Aouf, Nour-Eddine
Barbey, Carole
1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title_full 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title_fullStr 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title_full_unstemmed 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title_short 1,2,3,4-Tetra­hydro­isoquinoline-2-sulfonamide
title_sort 1,2,3,4-tetra­hydro­isoquinoline-2-sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960235/
https://www.ncbi.nlm.nih.gov/pubmed/21201459
http://dx.doi.org/10.1107/S1600536807068158
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