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N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate
The title compound, C(21)H(22)N(4)O(2)S(2)·0.5H(2)O, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the phenyl and imidazothiazole ring systems are 19.16 (9) and 21.37 (9)°. In the imidazothiazole ring systems, the cyclohexane rings adopt chair conformations, wh...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961240/ https://www.ncbi.nlm.nih.gov/pubmed/21202301 http://dx.doi.org/10.1107/S1600536808009306 |
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author | Akkurt, Mehmet Yalçın, Şerife Pınar Güzeldemirci, Nuray Ulusoy Büyükgüngör, Orhan |
author_facet | Akkurt, Mehmet Yalçın, Şerife Pınar Güzeldemirci, Nuray Ulusoy Büyükgüngör, Orhan |
author_sort | Akkurt, Mehmet |
collection | PubMed |
description | The title compound, C(21)H(22)N(4)O(2)S(2)·0.5H(2)O, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the phenyl and imidazothiazole ring systems are 19.16 (9) and 21.37 (9)°. In the imidazothiazole ring systems, the cyclohexane rings adopt chair conformations, while the thiazole rings have distorted envelope conformations. The two molecules are stabilized by intramolecular N—H⋯O, O—H⋯O and C—H⋯S interactions and the crystal structure is stabilized by intermolecular N—H⋯O, O—H⋯O, C—H⋯O and C—H⋯N interactions. |
format | Text |
id | pubmed-2961240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29612402010-12-30 N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate Akkurt, Mehmet Yalçın, Şerife Pınar Güzeldemirci, Nuray Ulusoy Büyükgüngör, Orhan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(22)N(4)O(2)S(2)·0.5H(2)O, crystallizes with two molecules in the asymmetric unit. The dihedral angles between the phenyl and imidazothiazole ring systems are 19.16 (9) and 21.37 (9)°. In the imidazothiazole ring systems, the cyclohexane rings adopt chair conformations, while the thiazole rings have distorted envelope conformations. The two molecules are stabilized by intramolecular N—H⋯O, O—H⋯O and C—H⋯S interactions and the crystal structure is stabilized by intermolecular N—H⋯O, O—H⋯O, C—H⋯O and C—H⋯N interactions. International Union of Crystallography 2008-04-10 /pmc/articles/PMC2961240/ /pubmed/21202301 http://dx.doi.org/10.1107/S1600536808009306 Text en © Akkurt et al. 2008 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 Yalçın, Şerife Pınar Güzeldemirci, Nuray Ulusoy Büyükgüngör, Orhan N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title |
N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title_full |
N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title_fullStr |
N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title_full_unstemmed |
N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title_short |
N-(3-Oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
title_sort | n-(3-oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-6-phenylimidazo[2,1-b][1,3]thiazole-3-acetamide hemihydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961240/ https://www.ncbi.nlm.nih.gov/pubmed/21202301 http://dx.doi.org/10.1107/S1600536808009306 |
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