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1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate
The title compound, C(13)H(14)N(2)OS(2)·H(2)O, appears in the form of bimolecular aggregate in which molecular components are linked by O—H⋯N hydrogen bonding. The nine-membered imidazo[1,2-a]pyridine system is almost planar, with a mean deviation of 0.026 (1) Å. An intramolecular C—H⋯O hydrogen b...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
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International Union of Crystallography
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969197/ https://www.ncbi.nlm.nih.gov/pubmed/21582952 http://dx.doi.org/10.1107/S1600536809023514 |
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| author | Bibila Mayaya Bisseyou, Yvon Sissouma, Drissa Goulizan Bi, Severin D. Ouattara, Mahama Yao-Kakou, R. C. A. |
| author_facet | Bibila Mayaya Bisseyou, Yvon Sissouma, Drissa Goulizan Bi, Severin D. Ouattara, Mahama Yao-Kakou, R. C. A. |
| author_sort | Bibila Mayaya Bisseyou, Yvon |
| collection | PubMed |
| description | The title compound, C(13)H(14)N(2)OS(2)·H(2)O, appears in the form of bimolecular aggregate in which molecular components are linked by O—H⋯N hydrogen bonding. The nine-membered imidazo[1,2-a]pyridine system is almost planar, with a mean deviation of 0.026 (1) Å. An intramolecular C—H⋯O hydrogen bond forms within the imidazo[1,2-a]pyridine system. The crystal packing is consolidated by O—H⋯O and C—H⋯O hydrogen bonds, forming a supramolecular structure consisting of perpendicular infinite molecular chains running along the a and c axes. |
| format | Text |
| id | pubmed-2969197 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2009 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29691972010-12-30 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate Bibila Mayaya Bisseyou, Yvon Sissouma, Drissa Goulizan Bi, Severin D. Ouattara, Mahama Yao-Kakou, R. C. A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(14)N(2)OS(2)·H(2)O, appears in the form of bimolecular aggregate in which molecular components are linked by O—H⋯N hydrogen bonding. The nine-membered imidazo[1,2-a]pyridine system is almost planar, with a mean deviation of 0.026 (1) Å. An intramolecular C—H⋯O hydrogen bond forms within the imidazo[1,2-a]pyridine system. The crystal packing is consolidated by O—H⋯O and C—H⋯O hydrogen bonds, forming a supramolecular structure consisting of perpendicular infinite molecular chains running along the a and c axes. International Union of Crystallography 2009-06-27 /pmc/articles/PMC2969197/ /pubmed/21582952 http://dx.doi.org/10.1107/S1600536809023514 Text en © Bibila Mayaya Bisseyou et al. 2009 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 Bibila Mayaya Bisseyou, Yvon Sissouma, Drissa Goulizan Bi, Severin D. Ouattara, Mahama Yao-Kakou, R. C. A. 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title | 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title_full | 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title_fullStr | 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title_full_unstemmed | 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title_short | 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| title_sort | 1-(2-methylimidazo[1,2-a]pyridin-3-yl)-3,3-bis(methylsulfanyl)prop-2-enone monohydrate |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969197/ https://www.ncbi.nlm.nih.gov/pubmed/21582952 http://dx.doi.org/10.1107/S1600536809023514 |
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