4-Benzylidene-2-methyl-11-phenyl-1,2,3,4,11,11a-hexahydropyrido[3,4-c][1,5]benzothiazepine
โ Scribed by Athimoolam, S. ;Kumar, R. Ranjith ;Kannan, R. Sayee ;Sridhar, B. ;Bahadur, S. Asath
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 659 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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โฆ Synopsis
In the title compound, C~26~H~24~N~2~S, the six- and seven-membered heterocyclic rings adopt half-chair and near-boat conformations, respectively. The molecular conformation is influenced by two weak intramolecular CโH...N interactions. The crystal structure is stablized by intermolecular CโH...N and CโH...ฯ interactions.
๐ SIMILAR VOLUMES
The molecule of the title compound, C~26~H~30~N~2~O~4~S, adopts a folded conformation, with the sulfonyl-bound benzene ring lying over the pyridinone ring [centroid-to-centroid distance = 3.893โ (1)โ ร ], forming a dihedral angle of 23.87โ (5)ยฐ. The pyrrolidine ring adopts a twist conformation and the d
The asymmetric unit of the title compound, C 26 H 30 N 2 O 4 S, consists of two independent molecules, A and B, with similar conformations. In both molecules, the pyrrolidine and dihydropyran rings adopt envelope conformations, and are trans-fused; the tosyl group is attached to the pyrrolidine ring
The mass spectrometric behaviour of seven tetrasubstituted 3a ,4,5,2,3d][1,5]benzothiazepines has been studied with the aid of mass-analysed ion kinetic energy spectrometry and exact mass measurements under electron impact ionization. All compounds show a tendency to eliminate a neutral substituted