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4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol
The title compound, C(20)H(23)Cl(2)NO, was prepared by condensation of (R)-1-(2-chlorophenyl)-1-cyclopentylmethanamine with 1-(5-chloro-2-hydroxyphenyl)ethanone, resulting in the formation of a new chiral center. The structural analysis confirms the absolute configuration of the title compound...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959664/ https://www.ncbi.nlm.nih.gov/pubmed/21581069 http://dx.doi.org/10.1107/S1600536808034624 |
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author | Zhang, Guang-You Yang, Ting Xu, Bao-Wang Chen, Di-Juan Wang, Wan-Hui |
author_facet | Zhang, Guang-You Yang, Ting Xu, Bao-Wang Chen, Di-Juan Wang, Wan-Hui |
author_sort | Zhang, Guang-You |
collection | PubMed |
description | The title compound, C(20)H(23)Cl(2)NO, was prepared by condensation of (R)-1-(2-chlorophenyl)-1-cyclopentylmethanamine with 1-(5-chloro-2-hydroxyphenyl)ethanone, resulting in the formation of a new chiral center. The structural analysis confirms the absolute configuration of the title compound and the formation of the (R,R) diastereoisomer. There is an intramolecular O—H⋯N hydrogen bond which stabilizes the conformation of the molecule. The molecules are linked to each other through weak C—H⋯π interactions. |
format | Text |
id | pubmed-2959664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29596642010-12-30 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol Zhang, Guang-You Yang, Ting Xu, Bao-Wang Chen, Di-Juan Wang, Wan-Hui Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(23)Cl(2)NO, was prepared by condensation of (R)-1-(2-chlorophenyl)-1-cyclopentylmethanamine with 1-(5-chloro-2-hydroxyphenyl)ethanone, resulting in the formation of a new chiral center. The structural analysis confirms the absolute configuration of the title compound and the formation of the (R,R) diastereoisomer. There is an intramolecular O—H⋯N hydrogen bond which stabilizes the conformation of the molecule. The molecules are linked to each other through weak C—H⋯π interactions. International Union of Crystallography 2008-10-25 /pmc/articles/PMC2959664/ /pubmed/21581069 http://dx.doi.org/10.1107/S1600536808034624 Text en © Zhang et al. 2008 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 Zhang, Guang-You Yang, Ting Xu, Bao-Wang Chen, Di-Juan Wang, Wan-Hui 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title | 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title_full | 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title_fullStr | 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title_full_unstemmed | 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title_short | 4-Chloro-2-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
title_sort | 4-chloro-2-((1r)-1-{[(r)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959664/ https://www.ncbi.nlm.nih.gov/pubmed/21581069 http://dx.doi.org/10.1107/S1600536808034624 |
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