Unknown

Dataset Information

0

Methyl 3'-benzyl-4'-(2,4-di-chloro-phen-yl)-1'-methyl-2-oxo-spiro-[indoline-3,2'-pyrrolidine]-3'-carboxyl-ate.


ABSTRACT: In the title compound, C27H24Cl2N2O3, the indole ring system is essentially planar, with a maximum deviation of 0.082?(2)?Å for the carbonyl C atom. It makes a dihedral angle of 88.53?(6)° with the mean plane of the 4-methyl-pyrrolidine ring, which adopts an envelope conformation with the N atom at the flap position. The mol-ecular structure is stabilized by intra-molecular C-H?O hydrogen bonds, which generate S(6) and S(7) ring motifs, and an intra-molecular ?-? inter-action involving the benzyl and di-chloro-substituted benzene rings [centroid-centroid distance = 3.6291?(11)?Å]. In the crystal, mol-ecules are linked via N-H?O hydrogen bonds, forming C(7) chains running parallel to [10-1].

SUBMITTER: Karthikeyan S 

PROVIDER: S-EPMC3998484 | biostudies-literature | 2014 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Methyl 3'-benzyl-4'-(2,4-di-chloro-phen-yl)-1'-methyl-2-oxo-spiro-[indoline-3,2'-pyrrolidine]-3'-carboxyl-ate.

Karthikeyan S S   Narayanan P P   Sethusankar K K   Devaraj Anthonisamy A   Bakthadoss Manickam M  

Acta crystallographica. Section E, Structure reports online 20140222 Pt 3


In the title compound, C27H24Cl2N2O3, the indole ring system is essentially planar, with a maximum deviation of 0.082 (2) Å for the carbonyl C atom. It makes a dihedral angle of 88.53 (6)° with the mean plane of the 4-methyl-pyrrolidine ring, which adopts an envelope conformation with the N atom at the flap position. The mol-ecular structure is stabilized by intra-molecular C-H⋯O hydrogen bonds, which generate S(6) and S(7) ring motifs, and an intra-molecular π-π inter-action involving the benzy  ...[more]

Similar Datasets

| S-EPMC3793722 | biostudies-literature
| S-EPMC3998486 | biostudies-literature
| S-EPMC4420098 | biostudies-literature
| S-EPMC3684914 | biostudies-literature
| S-EPMC3998463 | biostudies-literature
| S-EPMC3684912 | biostudies-literature
| S-EPMC3998460 | biostudies-literature
| S-EPMC4011217 | biostudies-literature
| S-EPMC3684913 | biostudies-literature
| S-EPMC3589042 | biostudies-literature