1-Cyclopentyl-4-(4-fluorophenyl)-7,7-dimethyl-4,6,7,8-tetrahydroquinoline-2,5-dione
✍ Scribed by Tu, Shujiang ;Zhu, Xiaotong ;Zhang, Jinpeng ;Xu, Jianing ;Wang, Qian
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 146 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 22 H 26 FNO 2 , was synthesized by the reaction of 4-fluorobenzaldehyde, Meldrum's acid, dimedone and cyclopentylamine hydrochloride, together with sodium acetate, in ethanol under microwave irradiation. The pyridone ring adopts a screw-boat conformation and the cyclohexenone ring an envelope conformation.
📜 SIMILAR VOLUMES
The title compound, C 20 H 22 ClNO 3 , was synthesized by the reaction of 3-chlorobenzaldehyde, 5,5-dimethyl-1,3-cyclohexanedione and methyl 2-aminocrotonate in an ionic liquid medium. The X-ray analysis reveals that the nitrogencontaining ring adopts a boat conformation and the cyclohexene ring has
The title compound, C 18 H 20 ClNO 2 , has been synthesized by the reaction of 4-chlorobenzaldehyde, Meldrum's acid, dimedone and CH 3 NH 3 Cl(NaOAc) in ethanol under microwave irradiation. The pyridone ring adopts a screw-boat conformation and the cyclohexenone ring an envelope conformation.
All the interatomic distances in the title compound, C 22 H 25 N 3 O 4 , are normal. The heteroatom ring of the quinoxalinone system shows a half-chair conformation, slightly distorted towards a sofa. In the crystal structure, the molecules dimerize via a pair of N-HÁ Á ÁO hydrogen bonds. The dimers