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Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate
In the title compound, C(27)H(28)N(2)O(4), the pyrrolidine ring adopts a twist conformation. The plane of the indole ring is almost perpendicular to that of the pyrrolidine ring, making a dihedral angle of 88.50 (6)°. The planes of the naphthyl ring system and the pyrrolidine ring are tilted by an a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011217/ https://www.ncbi.nlm.nih.gov/pubmed/24860349 http://dx.doi.org/10.1107/S1600536814007065 |
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author | Vijayakumar, Vinodhkumar Peters, Gunther H. Suresh, M. Raghavachary, Raghunathan Jagadeesan, G. |
author_facet | Vijayakumar, Vinodhkumar Peters, Gunther H. Suresh, M. Raghavachary, Raghunathan Jagadeesan, G. |
author_sort | Vijayakumar, Vinodhkumar |
collection | PubMed |
description | In the title compound, C(27)H(28)N(2)O(4), the pyrrolidine ring adopts a twist conformation. The plane of the indole ring is almost perpendicular to that of the pyrrolidine ring, making a dihedral angle of 88.50 (6)°. The planes of the naphthyl ring system and the pyrrolidine ring are tilted by an angle of 55.86 (5)°. The molecular conformation is stabilized by intramolecular O—H⋯O and O—H⋯N hydrogen bonds. |
format | Online Article Text |
id | pubmed-4011217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-40112172014-05-23 Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate Vijayakumar, Vinodhkumar Peters, Gunther H. Suresh, M. Raghavachary, Raghunathan Jagadeesan, G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(28)N(2)O(4), the pyrrolidine ring adopts a twist conformation. The plane of the indole ring is almost perpendicular to that of the pyrrolidine ring, making a dihedral angle of 88.50 (6)°. The planes of the naphthyl ring system and the pyrrolidine ring are tilted by an angle of 55.86 (5)°. The molecular conformation is stabilized by intramolecular O—H⋯O and O—H⋯N hydrogen bonds. International Union of Crystallography 2014-04-12 /pmc/articles/PMC4011217/ /pubmed/24860349 http://dx.doi.org/10.1107/S1600536814007065 Text en © Vijayakumar et al. 2014 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 Vijayakumar, Vinodhkumar Peters, Gunther H. Suresh, M. Raghavachary, Raghunathan Jagadeesan, G. Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title | Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title_full | Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title_fullStr | Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title_full_unstemmed | Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title_short | Methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
title_sort | methyl 1-ethyl-3′-[hydroxy(naphthalen-1-yl)methyl]-1′-methyl-2-oxospiro[indoline-3,2′-pyrrolidine]-3′-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011217/ https://www.ncbi.nlm.nih.gov/pubmed/24860349 http://dx.doi.org/10.1107/S1600536814007065 |
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