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Document Type |
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Article In Journal |
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Document Title |
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Pyridinium 5-[(1,3-diethyl-6-hydr-oxy-4-oxo-2-thioxo-1,2,3,4-tetra-hydro- pyrimidin-5-yl)(2-methoxy-phen-yl)meth-yl]-1,3-diethyl-4,6-dioxo-2- thioxopyrimidin-5-ide Pyridinium 5-[(1,3-diethyl-6-hydr-oxy-4-oxo-2-thioxo-1,2,3,4-tetra-hydro- pyrimidin-5-yl)(2-methoxy-phen-yl)meth-yl]-1,3-diethyl-4,6-dioxo-2- thioxopyrimidin-5-ide |
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Subject |
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Chemistry |
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Document Language |
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English |
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Abstract |
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1,3-Diethyl-2-thio-barbituric acid reacts with 2-anisaldehyde to form the Michael addition product 2-anisylbis(1,3-diethyl-2-thio-barbitur-5-yl)methanate, which crystallizes as the title pyridin-ium salt, C5H 6N+·C24H29N4O 5S2-, when it reacts with the pyridine used to catalyse the reaction. There are two independent ion pairs in the crystal structure. The anion features a methine C atom connected to three six-membered rings; one of the rings carries a hydr-oxy group, which engages in hydrogen bonding with the carbonyl group belonging to another ring. The monoclinic unit cell emulates an ortho-rhom-bic unit cell, and is a twin with a minor twin component of 35%. © 2009 Asiri et al. |
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ISSN |
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1600-5368 |
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Journal Name |
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Acta Crystallographica Section E: Structure Reports Online |
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Volume |
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65 |
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Issue Number |
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8 |
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Publishing Year |
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2009 AH
2009 AD |
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Article Type |
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Article |
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Added Date |
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Sunday, October 18, 2009 |
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Researchers
| عبدالله محمد أحمد عسيري | Abdullah Mohamed Asiri | Researcher | Doctorate | aasiri2@kau.edu.sa |
| سلمان أحمد خان | Salman Ahmad Khan | Researcher | Doctorate | sahmad_phd@yahoo.co.in |
| Ng, S.W | Ng, S.W | Researcher | Doctorate | seikweng@um.edu.my |
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