4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide

The title compound, C(15)H(11)FN(4)OS, is almost planar, the dihedral angle between the aromatic ring systems being 5.00 (13)°. The conformation is stabilized by intra­molecular N—H⋯N and N—H⋯O hydrogen bonds, which generate S(5) and S(6) rings, respectively. N—H⋯F and C—H⋯S inter­actions also occur...

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Detalles Bibliográficos
Autores principales: Pervez, Humayun, Yaqub, Muhammad, Ramzan, Muhammad, Iqbal, Mohammad S., Tahir, M. Nawaz
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979150/
https://www.ncbi.nlm.nih.gov/pubmed/21579082
http://dx.doi.org/10.1107/S1600536810011682
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author Pervez, Humayun
Yaqub, Muhammad
Ramzan, Muhammad
Iqbal, Mohammad S.
Tahir, M. Nawaz
author_facet Pervez, Humayun
Yaqub, Muhammad
Ramzan, Muhammad
Iqbal, Mohammad S.
Tahir, M. Nawaz
author_sort Pervez, Humayun
collection PubMed
description The title compound, C(15)H(11)FN(4)OS, is almost planar, the dihedral angle between the aromatic ring systems being 5.00 (13)°. The conformation is stabilized by intra­molecular N—H⋯N and N—H⋯O hydrogen bonds, which generate S(5) and S(6) rings, respectively. N—H⋯F and C—H⋯S inter­actions also occur. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops.
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spelling pubmed-29791502010-12-30 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide Pervez, Humayun Yaqub, Muhammad Ramzan, Muhammad Iqbal, Mohammad S. Tahir, M. Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(11)FN(4)OS, is almost planar, the dihedral angle between the aromatic ring systems being 5.00 (13)°. The conformation is stabilized by intra­molecular N—H⋯N and N—H⋯O hydrogen bonds, which generate S(5) and S(6) rings, respectively. N—H⋯F and C—H⋯S inter­actions also occur. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. International Union of Crystallography 2010-04-02 /pmc/articles/PMC2979150/ /pubmed/21579082 http://dx.doi.org/10.1107/S1600536810011682 Text en © Pervez 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
Pervez, Humayun
Yaqub, Muhammad
Ramzan, Muhammad
Iqbal, Mohammad S.
Tahir, M. Nawaz
4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title_full 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title_fullStr 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title_full_unstemmed 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title_short 4-(2-Fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
title_sort 4-(2-fluoro­phen­yl)-1-(2-oxoindolin-3-yl­idene)thio­semicarbazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979150/
https://www.ncbi.nlm.nih.gov/pubmed/21579082
http://dx.doi.org/10.1107/S1600536810011682
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AT iqbalmohammads 42fluorophenyl12oxoindolin3ylidenethiosemicarbazide
AT tahirmnawaz 42fluorophenyl12oxoindolin3ylidenethiosemicarbazide

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