Gliquidone

The title compound {systematic name: N-cyclo­hexyl­carba­moyl-4-[2-(7-meth­oxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetra­hydro­isoquinolin-2-yl)eth­yl]benzene­sulfonamide}, C(27)H(33)N(3)O(6)S, displays an intra­molecular N—H⋯O=S inter­action, as well as inter­molecular N—H⋯O=C hydrogen bonds. The latter...

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Detalles Bibliográficos
Autores principales: Gelbrich, Thomas, Haddow, Mairi F., Griesser, Ulrich J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120417/
https://www.ncbi.nlm.nih.gov/pubmed/21754738
http://dx.doi.org/10.1107/S1600536811016680
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author Gelbrich, Thomas
Haddow, Mairi F.
Griesser, Ulrich J.
author_facet Gelbrich, Thomas
Haddow, Mairi F.
Griesser, Ulrich J.
author_sort Gelbrich, Thomas
collection PubMed
description The title compound {systematic name: N-cyclo­hexyl­carba­moyl-4-[2-(7-meth­oxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetra­hydro­isoquinolin-2-yl)eth­yl]benzene­sulfonamide}, C(27)H(33)N(3)O(6)S, displays an intra­molecular N—H⋯O=S inter­action, as well as inter­molecular N—H⋯O=C hydrogen bonds. The latter inter­actions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonyl­urea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010 ▶). J. Phys. Chem. B, 114, 11603–11610].
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spelling pubmed-31204172011-07-13 Gliquidone Gelbrich, Thomas Haddow, Mairi F. Griesser, Ulrich J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound {systematic name: N-cyclo­hexyl­carba­moyl-4-[2-(7-meth­oxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetra­hydro­isoquinolin-2-yl)eth­yl]benzene­sulfonamide}, C(27)H(33)N(3)O(6)S, displays an intra­molecular N—H⋯O=S inter­action, as well as inter­molecular N—H⋯O=C hydrogen bonds. The latter inter­actions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonyl­urea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010 ▶). J. Phys. Chem. B, 114, 11603–11610]. International Union of Crystallography 2011-05-07 /pmc/articles/PMC3120417/ /pubmed/21754738 http://dx.doi.org/10.1107/S1600536811016680 Text en © Gelbrich et al. 2011 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
Gelbrich, Thomas
Haddow, Mairi F.
Griesser, Ulrich J.
Gliquidone
title Gliquidone
title_full Gliquidone
title_fullStr Gliquidone
title_full_unstemmed Gliquidone
title_short Gliquidone
title_sort gliquidone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120417/
https://www.ncbi.nlm.nih.gov/pubmed/21754738
http://dx.doi.org/10.1107/S1600536811016680
work_keys_str_mv AT gelbrichthomas gliquidone
AT haddowmairif gliquidone
AT griesserulrichj gliquidone

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