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4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide
In the title compound, C(16)H(14)N(4)O(2)S, intramolecular N—H⋯N hydrogen bonding forms an S(5) ring, whereas N—H⋯O and C—H⋯S interactions complete S(6) ring motifs. In the crystal, molecules form inversion dimers due to N—H⋯O interactions. The dimers are interlinked through N—H⋯S hydrogen bond...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979529/ https://www.ncbi.nlm.nih.gov/pubmed/21579483 http://dx.doi.org/10.1107/S1600536810018052 |
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author | Pervez, Humayun Iqbal, Mohammad S. Saira, Naveeda Yaqub, Muhammad Tahir, M. Nawaz |
author_facet | Pervez, Humayun Iqbal, Mohammad S. Saira, Naveeda Yaqub, Muhammad Tahir, M. Nawaz |
author_sort | Pervez, Humayun |
collection | PubMed |
description | In the title compound, C(16)H(14)N(4)O(2)S, intramolecular N—H⋯N hydrogen bonding forms an S(5) ring, whereas N—H⋯O and C—H⋯S interactions complete S(6) ring motifs. In the crystal, molecules form inversion dimers due to N—H⋯O interactions. The dimers are interlinked through N—H⋯S hydrogen bonds and π–π interactions occur with a centroid–centroid distance of 3.8422 (11) Å between the methoxy-containing benzene ring and the five-membered heterocyclic ring. |
format | Text |
id | pubmed-2979529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29795292010-12-30 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide Pervez, Humayun Iqbal, Mohammad S. Saira, Naveeda Yaqub, Muhammad Tahir, M. Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(14)N(4)O(2)S, intramolecular N—H⋯N hydrogen bonding forms an S(5) ring, whereas N—H⋯O and C—H⋯S interactions complete S(6) ring motifs. In the crystal, molecules form inversion dimers due to N—H⋯O interactions. The dimers are interlinked through N—H⋯S hydrogen bonds and π–π interactions occur with a centroid–centroid distance of 3.8422 (11) Å between the methoxy-containing benzene ring and the five-membered heterocyclic ring. International Union of Crystallography 2010-05-22 /pmc/articles/PMC2979529/ /pubmed/21579483 http://dx.doi.org/10.1107/S1600536810018052 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 Iqbal, Mohammad S. Saira, Naveeda Yaqub, Muhammad Tahir, M. Nawaz 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title | 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_full | 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_fullStr | 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_full_unstemmed | 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_short | 4-(3-Methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
title_sort | 4-(3-methoxyphenyl)-1-(2-oxoindolin-3-ylidene)thiosemicarbazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979529/ https://www.ncbi.nlm.nih.gov/pubmed/21579483 http://dx.doi.org/10.1107/S1600536810018052 |
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