2-Amino-4-(4-chlorophenyl)-6-morpholinopyridine-3,5-dicarbonitrile
✍ Scribed by Tu, Shu-Jiang ;Li, Tuan-Jie ;Zhu, Song-Lei ;Zou, Xiang ;Wang, Qian
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 328 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 17 H 14 ClN 5 O, was synthesized by the reaction of malononitrile with 4-chlorobenzaldehyde and morpholine in glycol under microwave irradiation. X-ray analysis reveals that the morpholine ring is in a chair conformation. In the crystal structure, intermolecular N-HÁ Á ÁO, C-HÁ Á ÁN and N-HÁ Á ÁN hydrogen bonds form a three-dimensional network.
📜 SIMILAR VOLUMES
In the title compound, C 24 H 25 Cl 2 N 2 O 3 P, the P atom adopts a distorted tetrahedral configuration. Weak intermolecular N-HÁ Á ÁN and C-HÁ Á ÁO hydrogen bonds are observed, and C-HÁ Á Á interactions also contribute to the crystal packing.
The title compound, C 23 H 26 ClN 5 O 2 , was synthesized by the reaction of 4- [(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine and 5-chloromethyl-3-(2-chlorophenyl)-1,2,4oxadiazole. In the structure, there are intramolecular C-HÁ Á ÁN, N-HÁ Á ÁN and C-HÁ Á ÁO hydrogen bonds, and intermolecular
In the title compound, C 24 H 20 ClN 3 O 3 , a bifurcated intramolecular N-HÁ Á Á(O,N) hydrogen bond helps to establish the molecular conformation.