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r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate

In the title compound, C(21)H(25)NO(3)·C(2)H(4)O(2), the piperidone ring adopts a chair conformation. The two meth­oxy groups are nearly coplanar with the aromatic rings to which they are attached. The dihedral angle between the two aromatic rings is 60.9 (2)°. There are two short intra­molecular N—...

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Detalles Bibliográficos
Autores principales: Aridoss, G., Sundaramoorthy, S., Velmurugan, D., Park, K. S., Jeong, Y. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979382/
https://www.ncbi.nlm.nih.gov/pubmed/21579504
http://dx.doi.org/10.1107/S1600536810017721
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author Aridoss, G.
Sundaramoorthy, S.
Velmurugan, D.
Park, K. S.
Jeong, Y. T.
author_facet Aridoss, G.
Sundaramoorthy, S.
Velmurugan, D.
Park, K. S.
Jeong, Y. T.
author_sort Aridoss, G.
collection PubMed
description In the title compound, C(21)H(25)NO(3)·C(2)H(4)O(2), the piperidone ring adopts a chair conformation. The two meth­oxy groups are nearly coplanar with the aromatic rings to which they are attached. The dihedral angle between the two aromatic rings is 60.9 (2)°. There are two short intra­molecular N—H⋯O contacts. The crystal packing is stabilized by inter­molecular O—H⋯N and C—H⋯O inter­actions.
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spelling pubmed-29793822010-12-30 r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate Aridoss, G. Sundaramoorthy, S. Velmurugan, D. Park, K. S. Jeong, Y. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(25)NO(3)·C(2)H(4)O(2), the piperidone ring adopts a chair conformation. The two meth­oxy groups are nearly coplanar with the aromatic rings to which they are attached. The dihedral angle between the two aromatic rings is 60.9 (2)°. There are two short intra­molecular N—H⋯O contacts. The crystal packing is stabilized by inter­molecular O—H⋯N and C—H⋯O inter­actions. International Union of Crystallography 2010-05-22 /pmc/articles/PMC2979382/ /pubmed/21579504 http://dx.doi.org/10.1107/S1600536810017721 Text en © Aridoss et al. 2010 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
Aridoss, G.
Sundaramoorthy, S.
Velmurugan, D.
Park, K. S.
Jeong, Y. T.
r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title_full r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title_fullStr r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title_full_unstemmed r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title_short r-2,c-6-Bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
title_sort r-2,c-6-bis(2-methoxy­phen­yl)-t-3,t-5-dimethyl­piperidin-4-one acetic acid solvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979382/
https://www.ncbi.nlm.nih.gov/pubmed/21579504
http://dx.doi.org/10.1107/S1600536810017721
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