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.

Detalles Bibliográficos
Autores principales: Gangadharan, Rajeswari, SethuSankar, K., Bakthadoss, Manickam, Sivakumar, Nagappan, Velmurugan, D.
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