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Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate

In the title compound, C(16)H(14)F(6)N(2)O(3), the dihydro­pyrimid­in­one ring adopts an envelope conformation. In the crystal, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds into a ribbon-like structure along the b axis. In the ribbon, a pair of bifurcated acceptor N—H⋯O and C—H⋯O bonds ge...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Babu, M., Kalluraya, B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969686/
https://www.ncbi.nlm.nih.gov/pubmed/21583249
http://dx.doi.org/10.1107/S1600536809019035
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author Fun, Hoong-Kun
Quah, Ching Kheng
Babu, M.
Kalluraya, B.
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Babu, M.
Kalluraya, B.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(16)H(14)F(6)N(2)O(3), the dihydro­pyrimid­in­one ring adopts an envelope conformation. In the crystal, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds into a ribbon-like structure along the b axis. In the ribbon, a pair of bifurcated acceptor N—H⋯O and C—H⋯O bonds generate an R (2) (1)(6) ring motif. Adjacent ribbons are linked via C—H⋯F hydrogen bonds.
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spelling pubmed-29696862010-12-30 Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate Fun, Hoong-Kun Quah, Ching Kheng Babu, M. Kalluraya, B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(14)F(6)N(2)O(3), the dihydro­pyrimid­in­one ring adopts an envelope conformation. In the crystal, mol­ecules are linked by N—H⋯O and C—H⋯O hydrogen bonds into a ribbon-like structure along the b axis. In the ribbon, a pair of bifurcated acceptor N—H⋯O and C—H⋯O bonds generate an R (2) (1)(6) ring motif. Adjacent ribbons are linked via C—H⋯F hydrogen bonds. International Union of Crystallography 2009-05-29 /pmc/articles/PMC2969686/ /pubmed/21583249 http://dx.doi.org/10.1107/S1600536809019035 Text en © Fun 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
Fun, Hoong-Kun
Quah, Ching Kheng
Babu, M.
Kalluraya, B.
Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title_full Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title_fullStr Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title_full_unstemmed Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title_short Ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
title_sort ethyl 4-[3,5-bis­(trifluoro­meth­yl)phen­yl]-6-methyl-2-oxo-1,2,3,4-tetra­hydro­pyrimidine-5-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969686/
https://www.ncbi.nlm.nih.gov/pubmed/21583249
http://dx.doi.org/10.1107/S1600536809019035
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