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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...

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Autores principales: Gaye, Papa Aly, Barry, Aliou Hamady, Gaye, Mohamed, Sarr, Aminata Diasse, Sall, Abdou Salam
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
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.
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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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