The indole moiety of the title compound, C 23 H 24 N 2 O 3 , is planar; but the pyrrolidine ring adopts an envelope conformation. The conformation is stabilized by intramolecular CÐ HÁ Á ÁO interactions and the packing of the molecules is stabilized by strong NÐHÁ Á ÁN hydrogen bonds.
1′-Methyl-4′-phenyl-1H-indole-3-spiro-2′-pyrrolidine-3′-spiro-1′′-cyclooctane-2(3H),2′′-dione
✍ Scribed by Kumar, R. Ganesh ;Gayathri, D. ;Velmurugan, D. ;Ravikumar, K. ;Poornachandran, M.
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 360 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
1 0 0 0 -Methyl-4 0 0 0 -phenyl-1H-indole-3-spiro-2 0 0 0 -pyrrolidine-3 0 0 0 -spiro-1 0 0 00 0 0 -cyclooctane-2(3H),2 0 0
📜 SIMILAR VOLUMES
In the title compound, C 26 H 27 NO 3 , the pyrrolidine ring adopts an envelope conformation. The indanedione group is planar, the dihedral angle between the fused five-and six-membered rings of this group being 1.1 (2) . There are intramolecular C-HÁ Á ÁO and C-HÁ Á Á interactions.
In the title compound, C 29 H 26 N 2 O 3 , the pyrrolidine ring adopts an envelope conformation and the cyclohexane ring adopts a chair conformation. The structure is stabilized by intramolecular CÐHÁ Á ÁO and %±% interactions.