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4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1)
In the title compound, C(6)H(9)N(2)S(+)·Cl(−)·CH(4)N(2)S, the 4,6-dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium cation is protonated at one of the pyrimidine N atoms. The cations are bridged by the chloride anions through a pair of N—H⋯Cl hydrogen bonds. The amino groups of each thiourea adduct i...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969793/ https://www.ncbi.nlm.nih.gov/pubmed/21583117 http://dx.doi.org/10.1107/S1600536809016857 |
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author | Gaye, Papa Aly Barry, Aliou Hamady Gaye, Mohamed Sarr, Aminata Diasse Sall, Abdou Salam |
author_facet | Gaye, Papa Aly Barry, Aliou Hamady Gaye, Mohamed Sarr, Aminata Diasse Sall, Abdou Salam |
author_sort | Gaye, Papa Aly |
collection | PubMed |
description | In the title compound, C(6)H(9)N(2)S(+)·Cl(−)·CH(4)N(2)S, the 4,6-dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium cation is protonated at one of the pyrimidine N atoms. The cations are bridged by the chloride anions through a pair of N—H⋯Cl hydrogen bonds. The amino groups of each thiourea adduct interact with the chloride anions through a pair of N—H⋯Cl hydrogen bonds and the S atom of another thiourea adduct through a pair of N—H⋯S hydrogen bonds. These interactions result in a layered hydrogen-bonded network propagating parallel to the bc plane. Except for two H atoms, all atoms are on special positions. |
format | Text |
id | pubmed-2969793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29697932010-12-30 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) Gaye, Papa Aly Barry, Aliou Hamady Gaye, Mohamed Sarr, Aminata Diasse Sall, Abdou Salam Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(6)H(9)N(2)S(+)·Cl(−)·CH(4)N(2)S, the 4,6-dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium cation is protonated at one of the pyrimidine N atoms. The cations are bridged by the chloride anions through a pair of N—H⋯Cl hydrogen bonds. The amino groups of each thiourea adduct interact with the chloride anions through a pair of N—H⋯Cl hydrogen bonds and the S atom of another thiourea adduct through a pair of N—H⋯S hydrogen bonds. These interactions result in a layered hydrogen-bonded network propagating parallel to the bc plane. Except for two H atoms, all atoms are on special positions. International Union of Crystallography 2009-05-14 /pmc/articles/PMC2969793/ /pubmed/21583117 http://dx.doi.org/10.1107/S1600536809016857 Text en © Gaye 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 Gaye, Papa Aly Barry, Aliou Hamady Gaye, Mohamed Sarr, Aminata Diasse Sall, Abdou Salam 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title | 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title_full | 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title_fullStr | 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title_full_unstemmed | 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title_short | 4,6-Dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
title_sort | 4,6-dimethyl-2-thioxo-1,2-dihydropyrimidin-3-ium chloride–thiourea (1/1) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969793/ https://www.ncbi.nlm.nih.gov/pubmed/21583117 http://dx.doi.org/10.1107/S1600536809016857 |
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