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1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one

In the title compound, C(22)H(23)Cl(2)NO(2), the piperidine ring adopts a twist-boat conformation. The phenyl rings substituted at the 2- and 6-positions of the piperidine ring subtend dihedral angles of 60.6 (2) and 84.2 (1)°, respectively, with the mean plane of the piperidine ring. In the crystal...

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Detalles Bibliográficos
Autores principales: Sugumar, P., Kayalvizhi, R., Mini, R., Ponnuswamy, S., Ponnuswamy, M. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793827/
https://www.ncbi.nlm.nih.gov/pubmed/24109414
http://dx.doi.org/10.1107/S1600536813019582
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author Sugumar, P.
Kayalvizhi, R.
Mini, R.
Ponnuswamy, S.
Ponnuswamy, M. N.
author_facet Sugumar, P.
Kayalvizhi, R.
Mini, R.
Ponnuswamy, S.
Ponnuswamy, M. N.
author_sort Sugumar, P.
collection PubMed
description In the title compound, C(22)H(23)Cl(2)NO(2), the piperidine ring adopts a twist-boat conformation. The phenyl rings substituted at the 2- and 6-positions of the piperidine ring subtend dihedral angles of 60.6 (2) and 84.2 (1)°, respectively, with the mean plane of the piperidine ring. In the crystal, mol­ecules are linked by C—H⋯O inter­actions into zigzag chains running along the c-axis direction.
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spelling pubmed-37938272013-10-09 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one Sugumar, P. Kayalvizhi, R. Mini, R. Ponnuswamy, S. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(23)Cl(2)NO(2), the piperidine ring adopts a twist-boat conformation. The phenyl rings substituted at the 2- and 6-positions of the piperidine ring subtend dihedral angles of 60.6 (2) and 84.2 (1)°, respectively, with the mean plane of the piperidine ring. In the crystal, mol­ecules are linked by C—H⋯O inter­actions into zigzag chains running along the c-axis direction. International Union of Crystallography 2013-07-27 /pmc/articles/PMC3793827/ /pubmed/24109414 http://dx.doi.org/10.1107/S1600536813019582 Text en © Sugumar et al. 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
Sugumar, P.
Kayalvizhi, R.
Mini, R.
Ponnuswamy, S.
Ponnuswamy, M. N.
1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title_full 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title_fullStr 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title_full_unstemmed 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title_short 1-Di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
title_sort 1-di­chloro­acetyl-t-3-isopropyl-r-2,c-6-di­phenyl­piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793827/
https://www.ncbi.nlm.nih.gov/pubmed/24109414
http://dx.doi.org/10.1107/S1600536813019582
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