2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime

The central ring of the title compound, C(28)H(32)N(2)O(3), exists in a chair conformation with an equatorial disposition of all the alkyl and aryl groups on the heterocycle. The para-anisyl groups on both sides of the secondary amino group are oriented at an angle of 54.75 (4)° with respect to each...

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Detalles Bibliográficos
Autores principales: Park, Dong Ho, Ramkumar, V., Parthiban, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275265/
https://www.ncbi.nlm.nih.gov/pubmed/22347121
http://dx.doi.org/10.1107/S1600536812002140
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author Park, Dong Ho
Ramkumar, V.
Parthiban, P.
author_facet Park, Dong Ho
Ramkumar, V.
Parthiban, P.
author_sort Park, Dong Ho
collection PubMed
description The central ring of the title compound, C(28)H(32)N(2)O(3), exists in a chair conformation with an equatorial disposition of all the alkyl and aryl groups on the heterocycle. The para-anisyl groups on both sides of the secondary amino group are oriented at an angle of 54.75 (4)° with respect to each other. The oxime derivative exists as an E isomer with the methyl substitution on one of the active methyl­ene centers of the mol­ecule. The crystal packing features weak C—H⋯O inter­actions.
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spelling pubmed-32752652012-02-15 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime Park, Dong Ho Ramkumar, V. Parthiban, P. Acta Crystallogr Sect E Struct Rep Online Organic Papers The central ring of the title compound, C(28)H(32)N(2)O(3), exists in a chair conformation with an equatorial disposition of all the alkyl and aryl groups on the heterocycle. The para-anisyl groups on both sides of the secondary amino group are oriented at an angle of 54.75 (4)° with respect to each other. The oxime derivative exists as an E isomer with the methyl substitution on one of the active methyl­ene centers of the mol­ecule. The crystal packing features weak C—H⋯O inter­actions. International Union of Crystallography 2012-01-25 /pmc/articles/PMC3275265/ /pubmed/22347121 http://dx.doi.org/10.1107/S1600536812002140 Text en © Park et al. 2012 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
Park, Dong Ho
Ramkumar, V.
Parthiban, P.
2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title_full 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title_fullStr 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title_full_unstemmed 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title_short 2,6-Bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one O-benzyl­oxime
title_sort 2,6-bis(4-meth­oxy­phen­yl)-1,3-dimethyl­piperidin-4-one o-benzyl­oxime
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275265/
https://www.ncbi.nlm.nih.gov/pubmed/22347121
http://dx.doi.org/10.1107/S1600536812002140
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AT parthibanp 26bis4methoxyphenyl13dimethylpiperidin4oneobenzyloxime

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