The title compound, C 21 H 20 ClN 3 O 2 , was synthesized by the reaction of 4-chlorobenzaldehyde and 3-(5,5-dimethyl-3-oxocyclohex-1-enylamino)propanoic acid with malononitrile in ethylene glycol under microwave irradiation. The dihydropyridine ring has a boat conformation. The pyrimidine ring adop
8-(4-Chlorophenyl)-11,11-dimethyl-5,9-dioxo-6,8,9,10,11,12-hexahydro-5H-quinolino[1,2-a]quinazoline-7-carbonitrile N,N-dimethylformamide solvate
β Scribed by Jiang, Hong ;Wu, Shanshan ;Li, Chunmei
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 621 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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β¦ Synopsis
The title compound, C 25 H 20 ClN 3 O 2 ΓC 3 H 7 NO, was synthesized by the reaction of 4-chlorobenzaldehyde, 2-(5,5-dimethyl-3oxocyclohex-1-enylamino)benzoic acid and malononitrile in ethylene glycol under microwave irradiation. The dihydropyridine and pyrimidine rings both adopt boat conformations. The cyclohexene ring adopts an envelope conformation. In the crystal structure, the main molecules exist as N-HΓ Γ ΓO hydrogen-bonded dimers. The crystal packing is further stabilized by C-HΓ Γ ΓO and C-HΓ Γ Γ interactions. The N,N-dimethylformamide molecules lie within a channel formed by the quinolino[1,2-a]quinazoline molecules.
π SIMILAR VOLUMES
In the title compound, C 13 H 15 N 3 O 2 , the triazepane ring adopts a twist-boat conformation and the piperidine ring adopts a boat conformation. The molecular packing is stabilized by N-HΓ Γ ΓO, C-HΓ Γ ΓO, C-HΓ Γ Γ and van der Waals interactions.
In the molecule of the title compound, C~19~H~18~N~6~O~10~, the 2,8-dimethoxy-4,10-dimethyl-1,3,7,9-tetranitro analogue of TrΓΆger's base, the diazocine bridge imparts a twist such that the two aryl rings are offset with respect to one another. The hinge angle of the molecule, measured as the dihedra