5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione

The title compound, C(15)H(18)N(4)O(7), is a product of the substitution reaction of 5,5-di­bromo-1,3-di­methyl­barbituric acid with sodium sulfide in aqueous acetone. In the crystal, mol­ecules display neither inter­molecular nor intra­molecular hydrogen bonding and the two barbiturate rings adopt...

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Detalles Bibliográficos
Autores principales: Sweidan, Kamal, Steimann, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793818/
https://www.ncbi.nlm.nih.gov/pubmed/24109405
http://dx.doi.org/10.1107/S1600536813020138
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author Sweidan, Kamal
Steimann, Manfred
author_facet Sweidan, Kamal
Steimann, Manfred
author_sort Sweidan, Kamal
collection PubMed
description The title compound, C(15)H(18)N(4)O(7), is a product of the substitution reaction of 5,5-di­bromo-1,3-di­methyl­barbituric acid with sodium sulfide in aqueous acetone. In the crystal, mol­ecules display neither inter­molecular nor intra­molecular hydrogen bonding and the two barbiturate rings adopt the keto form.
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spelling pubmed-37938182013-10-09 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione Sweidan, Kamal Steimann, Manfred Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(18)N(4)O(7), is a product of the substitution reaction of 5,5-di­bromo-1,3-di­methyl­barbituric acid with sodium sulfide in aqueous acetone. In the crystal, mol­ecules display neither inter­molecular nor intra­molecular hydrogen bonding and the two barbiturate rings adopt the keto form. International Union of Crystallography 2013-07-27 /pmc/articles/PMC3793818/ /pubmed/24109405 http://dx.doi.org/10.1107/S1600536813020138 Text en © Sweidan and Steimann 2013 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
Sweidan, Kamal
Steimann, Manfred
5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title_full 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title_fullStr 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title_full_unstemmed 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title_short 5-[1-(1,3-Dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1H,3H,5H)-trione
title_sort 5-[1-(1,3-dimethyl-2,4,6-trioxohexa­hydropyrimidin-5-yl)-2-oxoprop­yl]-1,3-di­methyl­pyrimidine-2,4,6(1h,3h,5h)-trione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793818/
https://www.ncbi.nlm.nih.gov/pubmed/24109405
http://dx.doi.org/10.1107/S1600536813020138
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AT steimannmanfred 5113dimethyl246trioxohexahydropyrimidin5yl2oxopropyl13dimethylpyrimidine2461h3h5htrione

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