3-Carbamoyl-2,2,5,5-tetramethylpyrrolidin-1-yl acetate
✍ Scribed by Liu, Yang-Ping ;Zhang, Xiu-Feng ;Liu, Ke-Jian ;Liu, Yang
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 130 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title compound, C 11 H 20 N 2 O 3 , the pyrrolidine ring adopts an envelope conformation, where the acetoxy and carbamoyl groups are equatorial. Each molecule interacts, through strong N-HÁ Á ÁO hydrogen bonds, with two adjacent molecules.
📜 SIMILAR VOLUMES
In the title compound, C~18~H~18~ClN~3~O~3~, the pyrrolidine ring adopts an envelope conformation. The dihedral angle between the phenyl ring and the pyridine ring is 28.30 (7)°. The crystal packing is stabilized by N—H...O and C—H...O hydrogen bonding.
The title compound, C~26~H~26~N~2~O~7~, is a thiamidine derivative. Geometric parameters are in the usual ranges. The crystal packing is stabilized by a classical N—H...O hydrogen bond, several weak C—H...O hydrogen bonds and a π–π stacking interaction.
The title compound, C 18 H 28 N 2 , with a crystallographic twofold rotation axis, can function as a C 2 -symmetric diamine ligand.
In the title compound, C 11 H 18 N 2 O 2 S, the dihedral angle between the thiophene ring and the mean plane of the puckered imidazolidine ring is 85.0 (2) . Adjacent molecules are linked by pairs of inversion-related O-HÁ Á ÁN hydrogen bonds, leading to a chain structure.