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(4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate

The asymmetric unit of the title compound, C(16)H(13)N(3)O(3)·0.5C(2)H(6)OS, is composed of two independent pyrazolidine-3,5-dione mol­ecules and one dimethyl sulfoxide solvent mol­ecule. In each pyrazolidine-3,5-dione mol­ecule, an intra­molecular N—H⋯O hydrogen bond forms an S(5)S(6) motif. In the...

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Autores principales: Akkurt, Mehmet, Mohamed, Shaaban K., Elremaily, Mahmoud A. A., Ahmed, Eman. A., Albayati, Mustafa R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884425/
https://www.ncbi.nlm.nih.gov/pubmed/24427046
http://dx.doi.org/10.1107/S1600536813022034
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author Akkurt, Mehmet
Mohamed, Shaaban K.
Elremaily, Mahmoud A. A.
Ahmed, Eman. A.
Albayati, Mustafa R.
author_facet Akkurt, Mehmet
Mohamed, Shaaban K.
Elremaily, Mahmoud A. A.
Ahmed, Eman. A.
Albayati, Mustafa R.
author_sort Akkurt, Mehmet
collection PubMed
description The asymmetric unit of the title compound, C(16)H(13)N(3)O(3)·0.5C(2)H(6)OS, is composed of two independent pyrazolidine-3,5-dione mol­ecules and one dimethyl sulfoxide solvent mol­ecule. In each pyrazolidine-3,5-dione mol­ecule, an intra­molecular N—H⋯O hydrogen bond forms an S(5)S(6) motif. In the crystal, pairs of each independent pyrazolidine-3,5-dione mol­ecule are linked by N—H⋯O hydrogen bonds, forming dimers with R (2) (2)(8) motifs. These dimers are connected with the other mol­ecules through the solvent mol­ecules via O—H⋯O hydrogen bonds, forming ribbons along the b-axis direction. C—H⋯π inter­actions connect the ribbons. C—H⋯O interactions also occur.
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spelling pubmed-38844252014-01-14 (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate Akkurt, Mehmet Mohamed, Shaaban K. Elremaily, Mahmoud A. A. Ahmed, Eman. A. Albayati, Mustafa R. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(16)H(13)N(3)O(3)·0.5C(2)H(6)OS, is composed of two independent pyrazolidine-3,5-dione mol­ecules and one dimethyl sulfoxide solvent mol­ecule. In each pyrazolidine-3,5-dione mol­ecule, an intra­molecular N—H⋯O hydrogen bond forms an S(5)S(6) motif. In the crystal, pairs of each independent pyrazolidine-3,5-dione mol­ecule are linked by N—H⋯O hydrogen bonds, forming dimers with R (2) (2)(8) motifs. These dimers are connected with the other mol­ecules through the solvent mol­ecules via O—H⋯O hydrogen bonds, forming ribbons along the b-axis direction. C—H⋯π inter­actions connect the ribbons. C—H⋯O interactions also occur. International Union of Crystallography 2013-08-10 /pmc/articles/PMC3884425/ /pubmed/24427046 http://dx.doi.org/10.1107/S1600536813022034 Text en © Akkurt et al. 2013 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
Akkurt, Mehmet
Mohamed, Shaaban K.
Elremaily, Mahmoud A. A.
Ahmed, Eman. A.
Albayati, Mustafa R.
(4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title_full (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title_fullStr (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title_full_unstemmed (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title_short (4E)-4-[(2-Hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
title_sort (4e)-4-[(2-hy­droxy­anilino)methyl­idene]-1-phenyl­pyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884425/
https://www.ncbi.nlm.nih.gov/pubmed/24427046
http://dx.doi.org/10.1107/S1600536813022034
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