Cargando…
3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one
The title compound, C(20)H(21)N(3)O(4), crystallizes with two molecules in the asymmetric unit. In both molecules, the pyrrolidine ring adopts an envelope conformation. The crystal structure is stabilized by intermolecular C—H⋯O, N—H⋯O and O—H⋯O hydrogen bonds.
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009029/ https://www.ncbi.nlm.nih.gov/pubmed/21589106 http://dx.doi.org/10.1107/S1600536810041917 |
_version_ | 1782194588587393024 |
---|---|
author | Gangadharan, Rajeswari SethuSankar, K. Bakthadoss, Manickam Sivakumar, Nagappan Velmurugan, D. |
author_facet | Gangadharan, Rajeswari SethuSankar, K. Bakthadoss, Manickam Sivakumar, Nagappan Velmurugan, D. |
author_sort | Gangadharan, Rajeswari |
collection | PubMed |
description | The title compound, C(20)H(21)N(3)O(4), crystallizes with two molecules in the asymmetric unit. In both molecules, the pyrrolidine ring adopts an envelope conformation. The crystal structure is stabilized by intermolecular C—H⋯O, N—H⋯O and O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-3009029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30090292010-12-30 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one Gangadharan, Rajeswari SethuSankar, K. Bakthadoss, Manickam Sivakumar, Nagappan Velmurugan, D. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(21)N(3)O(4), crystallizes with two molecules in the asymmetric unit. In both molecules, the pyrrolidine ring adopts an envelope conformation. The crystal structure is stabilized by intermolecular C—H⋯O, N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2010-10-23 /pmc/articles/PMC3009029/ /pubmed/21589106 http://dx.doi.org/10.1107/S1600536810041917 Text en © Gangadharan 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 Gangadharan, Rajeswari SethuSankar, K. Bakthadoss, Manickam Sivakumar, Nagappan Velmurugan, D. 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title | 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title_full | 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title_fullStr | 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title_full_unstemmed | 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title_short | 3′-Hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
title_sort | 3′-hydroxymethyl-1′-methyl-3′-nitro-4′-(o-tolyl)spiro[indoline-3,2′-pyrrolidin]-2-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009029/ https://www.ncbi.nlm.nih.gov/pubmed/21589106 http://dx.doi.org/10.1107/S1600536810041917 |
work_keys_str_mv | AT gangadharanrajeswari 3hydroxymethyl1methyl3nitro4otolylspiroindoline32pyrrolidin2one AT sethusankark 3hydroxymethyl1methyl3nitro4otolylspiroindoline32pyrrolidin2one AT bakthadossmanickam 3hydroxymethyl1methyl3nitro4otolylspiroindoline32pyrrolidin2one AT sivakumarnagappan 3hydroxymethyl1methyl3nitro4otolylspiroindoline32pyrrolidin2one AT velmurugand 3hydroxymethyl1methyl3nitro4otolylspiroindoline32pyrrolidin2one |