Cargando…
Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate
In the title compound, C(18)H(22)ClNO(5), the cyclohexene ring adopts a distorted half-chair conformation. The molecular structure is stabilized by pairs of intramolecular N—H⋯O and O—H⋯O interactions, generating S(6) motifs. In the crystal, the molecules are linked by intermolecular C—H⋯O int...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120530/ https://www.ncbi.nlm.nih.gov/pubmed/21754804 http://dx.doi.org/10.1107/S1600536811017089 |
_version_ | 1782206700033409024 |
---|---|
author | Amirthaganesan, S. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. |
author_facet | Amirthaganesan, S. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. |
author_sort | Amirthaganesan, S. |
collection | PubMed |
description | In the title compound, C(18)H(22)ClNO(5), the cyclohexene ring adopts a distorted half-chair conformation. The molecular structure is stabilized by pairs of intramolecular N—H⋯O and O—H⋯O interactions, generating S(6) motifs. In the crystal, the molecules are linked by intermolecular C—H⋯O interactions, forming centrosymmetric dimers. |
format | Online Article Text |
id | pubmed-3120530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-31205302011-07-13 Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate Amirthaganesan, S. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(22)ClNO(5), the cyclohexene ring adopts a distorted half-chair conformation. The molecular structure is stabilized by pairs of intramolecular N—H⋯O and O—H⋯O interactions, generating S(6) motifs. In the crystal, the molecules are linked by intermolecular C—H⋯O interactions, forming centrosymmetric dimers. International Union of Crystallography 2011-05-14 /pmc/articles/PMC3120530/ /pubmed/21754804 http://dx.doi.org/10.1107/S1600536811017089 Text en © Amirthaganesan 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 Amirthaganesan, S. Sundaramoorthy, S. Velmurugan, D. Jeong, Y. T. Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title | Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title_full | Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title_fullStr | Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title_full_unstemmed | Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title_short | Dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
title_sort | dimethyl 2-(3-chlorophenyl)-6-hydroxy-6-methyl-4-(methylamino)cyclohex-3-ene-1,3-dicarboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120530/ https://www.ncbi.nlm.nih.gov/pubmed/21754804 http://dx.doi.org/10.1107/S1600536811017089 |
work_keys_str_mv | AT amirthaganesans dimethyl23chlorophenyl6hydroxy6methyl4methylaminocyclohex3ene13dicarboxylate AT sundaramoorthys dimethyl23chlorophenyl6hydroxy6methyl4methylaminocyclohex3ene13dicarboxylate AT velmurugand dimethyl23chlorophenyl6hydroxy6methyl4methylaminocyclohex3ene13dicarboxylate AT jeongyt dimethyl23chlorophenyl6hydroxy6methyl4methylaminocyclohex3ene13dicarboxylate |