(E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one

In the title compound, C(17)H(13)N(3)OS, the dihedral angle between the ring systems is 2.22 (5)°. The N—H grouping participates in both intra- and intermolecular N—H⋯O hydrogen bonds, the latter leading to dimers related by a twofold rotation axis.

Detalles Bibliográficos
Autores principales: Chakibe, Imane, Zerzouf, Abdelfettah, Essassi, El Mokhtar, Reichelt, Martin, Reuter, Hans
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979087/
https://www.ncbi.nlm.nih.gov/pubmed/21579149
http://dx.doi.org/10.1107/S1600536810013176
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author Chakibe, Imane
Zerzouf, Abdelfettah
Essassi, El Mokhtar
Reichelt, Martin
Reuter, Hans
author_facet Chakibe, Imane
Zerzouf, Abdelfettah
Essassi, El Mokhtar
Reichelt, Martin
Reuter, Hans
author_sort Chakibe, Imane
collection PubMed
description In the title compound, C(17)H(13)N(3)OS, the dihedral angle between the ring systems is 2.22 (5)°. The N—H grouping participates in both intra- and intermolecular N—H⋯O hydrogen bonds, the latter leading to dimers related by a twofold rotation axis.
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spelling pubmed-29790872010-12-30 (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one Chakibe, Imane Zerzouf, Abdelfettah Essassi, El Mokhtar Reichelt, Martin Reuter, Hans Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(13)N(3)OS, the dihedral angle between the ring systems is 2.22 (5)°. The N—H grouping participates in both intra- and intermolecular N—H⋯O hydrogen bonds, the latter leading to dimers related by a twofold rotation axis. International Union of Crystallography 2010-04-17 /pmc/articles/PMC2979087/ /pubmed/21579149 http://dx.doi.org/10.1107/S1600536810013176 Text en © Chakibe 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
Chakibe, Imane
Zerzouf, Abdelfettah
Essassi, El Mokhtar
Reichelt, Martin
Reuter, Hans
(E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_full (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_fullStr (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_full_unstemmed (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_short (E)-4-(2,3-Dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
title_sort (e)-4-(2,3-dihydro-1,3-benzothia­zol-2-yl­idene)-3-methyl-1-phenyl-1h-pyrazol-5(4h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979087/
https://www.ncbi.nlm.nih.gov/pubmed/21579149
http://dx.doi.org/10.1107/S1600536810013176
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