1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione

1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione

The title compound, C20H17N3O2S2, crystallizes with two molecules in the asymmetric unit. The pyrrolodine rings have envelope conformations in both molecules, the N atoms deviating by 0.574 (3) and 0.612 (2) Å from the mean planes through the ot...

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Main Authors: Sampath Natarajan, Rita Mathews
Format: Article
Language:English
Published: International Union of Crystallography 2012-02-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536811056236
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spelling doaj-1f5b4be4d91a4cecac2ebe1a438e55d42020-11-24T21:25:46ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-02-01682o343o34310.1107/S16005368110562361′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dioneSampath NatarajanRita MathewsThe title compound, C20H17N3O2S2, crystallizes with two molecules in the asymmetric unit. The pyrrolodine rings have envelope conformations in both molecules, the N atoms deviating by 0.574 (3) and 0.612 (2) Å from the mean planes through the other ring atoms. The 1′-methyl and 4′-phenyl groups on the pyrrolidine rings are substituted in equatorial positions. In the crystal, molecules are linked into a three-dimensional network by N—H...O, N—H...N and C—H...O and N—H...π hydrogen bonds. http://scripts.iucr.org/cgi-bin/paper?S1600536811056236
collection DOAJ
language English
format Article
sources DOAJ
author Sampath Natarajan
Rita Mathews
spellingShingle Sampath Natarajan
Rita Mathews
1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
Acta Crystallographica Section E
author_facet Sampath Natarajan
Rita Mathews
author_sort Sampath Natarajan
title 1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
title_short 1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
title_full 1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
title_fullStr 1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
title_full_unstemmed 1′-Methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
title_sort 1′-methyl-4′-phenyl-2′′-sulfanylidenedispiro[indoline-3,2′-pyrrolidine-3′,5′′-1,3-thiazolidine]-2,4′′-dione
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2012-02-01
description The title compound, C20H17N3O2S2, crystallizes with two molecules in the asymmetric unit. The pyrrolodine rings have envelope conformations in both molecules, the N atoms deviating by 0.574 (3) and 0.612 (2) Å from the mean planes through the other ring atoms. The 1′-methyl and 4′-phenyl groups on the pyrrolidine rings are substituted in equatorial positions. In the crystal, molecules are linked into a three-dimensional network by N—H...O, N—H...N and C—H...O and N—H...π hydrogen bonds.
url http://scripts.iucr.org/cgi-bin/paper?S1600536811056236
work_keys_str_mv AT sampathnatarajan 1amp8242methyl4amp8242phenyl2amp8242amp8242sulfanylidenedispiroindoline32amp8242pyrrolidine3amp82425amp8242amp824213thiazolidine24amp8242amp8242dione
AT ritamathews 1amp8242methyl4amp8242phenyl2amp8242amp8242sulfanylidenedispiroindoline32amp8242pyrrolidine3amp82425amp8242amp824213thiazolidine24amp8242amp8242dione
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