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4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione
In the title compound, C(27)H(20)ClNO(3), the two cyclopentane rings adopt envelope conformations. The pyrrolidine ring also adopts an envelope conformation (with the spiro C atom as the flap) and its least-squares plane (fitted to five atoms) makes dihedral angles of 66.50 (9), 77.36 (8) and 73.76...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200810/ https://www.ncbi.nlm.nih.gov/pubmed/22064509 http://dx.doi.org/10.1107/S1600536811033642 |
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author | Wei, Ang Chee Ali, Mohamed Ashraf Yoon, Yeong Keng Quah, Ching Kheng Fun, Hoong-Kun |
author_facet | Wei, Ang Chee Ali, Mohamed Ashraf Yoon, Yeong Keng Quah, Ching Kheng Fun, Hoong-Kun |
author_sort | Wei, Ang Chee |
collection | PubMed |
description | In the title compound, C(27)H(20)ClNO(3), the two cyclopentane rings adopt envelope conformations. The pyrrolidine ring also adopts an envelope conformation (with the spiro C atom as the flap) and its least-squares plane (fitted to five atoms) makes dihedral angles of 66.50 (9), 77.36 (8) and 73.76 (8)° with the chlorobenzene ring and the two 2,3-dihydro-1H-indene ring systems, respectively. The molecular conformation is stabilized by an intramolecular C—H⋯O hydrogen bond, which generates an S(6) ring motif. In the crystal, molecules are linked by C—H⋯O hydrogen bonds into chains running parallel to the [001] direction. |
format | Online Article Text |
id | pubmed-3200810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32008102011-11-06 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione Wei, Ang Chee Ali, Mohamed Ashraf Yoon, Yeong Keng Quah, Ching Kheng Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(20)ClNO(3), the two cyclopentane rings adopt envelope conformations. The pyrrolidine ring also adopts an envelope conformation (with the spiro C atom as the flap) and its least-squares plane (fitted to five atoms) makes dihedral angles of 66.50 (9), 77.36 (8) and 73.76 (8)° with the chlorobenzene ring and the two 2,3-dihydro-1H-indene ring systems, respectively. The molecular conformation is stabilized by an intramolecular C—H⋯O hydrogen bond, which generates an S(6) ring motif. In the crystal, molecules are linked by C—H⋯O hydrogen bonds into chains running parallel to the [001] direction. International Union of Crystallography 2011-08-27 /pmc/articles/PMC3200810/ /pubmed/22064509 http://dx.doi.org/10.1107/S1600536811033642 Text en © Wei 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 Wei, Ang Chee Ali, Mohamed Ashraf Yoon, Yeong Keng Quah, Ching Kheng Fun, Hoong-Kun 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title | 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_full | 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_fullStr | 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_full_unstemmed | 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_short | 4′-(4-Chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
title_sort | 4′-(4-chlorophenyl)-1′-methyldispiro[indan-2,2′-pyrrolidine-3′,2′′-indan]-1,3,1′′-trione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200810/ https://www.ncbi.nlm.nih.gov/pubmed/22064509 http://dx.doi.org/10.1107/S1600536811033642 |
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