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Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid

The title compound, C(21)H(21)NO(5), crystallizes with two mol­ecules in the asymmetric unit. In each mol­ecule, the central 1,4-di­hydro­pyridine ring adopts a shallow sofa conformations (with the C atom bearing the phenol ring as the flap), whereas the pendant cyclo­hexene rings both have twisted-...

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Autores principales: Akkurt, Mehmet, Jasinski, Jerry P., Mohamed, Shaaban K., Allah, Omyma A. Abd, Tamam, Asmaa H. A., Albayati, Mustafa R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719924/
https://www.ncbi.nlm.nih.gov/pubmed/26870552
http://dx.doi.org/10.1107/S2056989015021611
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author Akkurt, Mehmet
Jasinski, Jerry P.
Mohamed, Shaaban K.
Allah, Omyma A. Abd
Tamam, Asmaa H. A.
Albayati, Mustafa R.
author_facet Akkurt, Mehmet
Jasinski, Jerry P.
Mohamed, Shaaban K.
Allah, Omyma A. Abd
Tamam, Asmaa H. A.
Albayati, Mustafa R.
author_sort Akkurt, Mehmet
collection PubMed
description The title compound, C(21)H(21)NO(5), crystallizes with two mol­ecules in the asymmetric unit. In each mol­ecule, the central 1,4-di­hydro­pyridine ring adopts a shallow sofa conformations (with the C atom bearing the phenol ring as the flap), whereas the pendant cyclo­hexene rings both have twisted-boat conformations. Each mol­ecule features an intra­molecular O—H⋯O hydrogen bond, which closes an S(8) ring. In the crystal, the mol­ecules are linked by O—H⋯O, C—H⋯O and C—H⋯π inter­actions, forming a three-dimensional network.
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spelling pubmed-47199242016-02-11 Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid Akkurt, Mehmet Jasinski, Jerry P. Mohamed, Shaaban K. Allah, Omyma A. Abd Tamam, Asmaa H. A. Albayati, Mustafa R. Acta Crystallogr E Crystallogr Commun Data Reports The title compound, C(21)H(21)NO(5), crystallizes with two mol­ecules in the asymmetric unit. In each mol­ecule, the central 1,4-di­hydro­pyridine ring adopts a shallow sofa conformations (with the C atom bearing the phenol ring as the flap), whereas the pendant cyclo­hexene rings both have twisted-boat conformations. Each mol­ecule features an intra­molecular O—H⋯O hydrogen bond, which closes an S(8) ring. In the crystal, the mol­ecules are linked by O—H⋯O, C—H⋯O and C—H⋯π inter­actions, forming a three-dimensional network. International Union of Crystallography 2015-11-21 /pmc/articles/PMC4719924/ /pubmed/26870552 http://dx.doi.org/10.1107/S2056989015021611 Text en © Akkurt et al. 2015 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 Data Reports
Akkurt, Mehmet
Jasinski, Jerry P.
Mohamed, Shaaban K.
Allah, Omyma A. Abd
Tamam, Asmaa H. A.
Albayati, Mustafa R.
Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title_full Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title_fullStr Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title_full_unstemmed Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title_short Crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
title_sort crystal structure of 2-[9-(2-hy­droxy­phen­yl)-1,8-dioxo-1,2,3,4,5,6,7,8,9,10-deca­hydro­acridin-10-yl]acetic acid
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719924/
https://www.ncbi.nlm.nih.gov/pubmed/26870552
http://dx.doi.org/10.1107/S2056989015021611
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