N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide

In the title compound, C(19)H(20)ClN(3)O(3)S, the benzene ring is inclined to the indazole ring system by 51.23 (8)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers which stack in columns parallel to [011]. The atoms in the allyl group are disordered...

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Detalles Bibliográficos
Autores principales: Chicha, Hakima, Rakib, El Mostapha, Bouissane, Latifa, Saadi, Mohamed, El Ammari, Lahcen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051038/
https://www.ncbi.nlm.nih.gov/pubmed/24940237
http://dx.doi.org/10.1107/S1600536814010253
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author Chicha, Hakima
Rakib, El Mostapha
Bouissane, Latifa
Saadi, Mohamed
El Ammari, Lahcen
author_facet Chicha, Hakima
Rakib, El Mostapha
Bouissane, Latifa
Saadi, Mohamed
El Ammari, Lahcen
author_sort Chicha, Hakima
collection PubMed
description In the title compound, C(19)H(20)ClN(3)O(3)S, the benzene ring is inclined to the indazole ring system by 51.23 (8)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers which stack in columns parallel to [011]. The atoms in the allyl group are disordered over two sets of sites with an occupancy ratio of 0.624 (8):0.376 (8).
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spelling pubmed-40510382014-06-17 N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide Chicha, Hakima Rakib, El Mostapha Bouissane, Latifa Saadi, Mohamed El Ammari, Lahcen Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(20)ClN(3)O(3)S, the benzene ring is inclined to the indazole ring system by 51.23 (8)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers which stack in columns parallel to [011]. The atoms in the allyl group are disordered over two sets of sites with an occupancy ratio of 0.624 (8):0.376 (8). International Union of Crystallography 2014-05-10 /pmc/articles/PMC4051038/ /pubmed/24940237 http://dx.doi.org/10.1107/S1600536814010253 Text en © Chicha et al. 2014 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
Chicha, Hakima
Rakib, El Mostapha
Bouissane, Latifa
Saadi, Mohamed
El Ammari, Lahcen
N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title_full N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title_fullStr N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title_short N-(1-Allyl-3-chloro-4-eth­oxy-1H-indazol-5-yl)-4-methyl­benzene­sulfonamide
title_sort n-(1-allyl-3-chloro-4-eth­oxy-1h-indazol-5-yl)-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051038/
https://www.ncbi.nlm.nih.gov/pubmed/24940237
http://dx.doi.org/10.1107/S1600536814010253
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