Methyl 2-amino-4-(3-fluorophenyl)-4H-benzo[h]chromene-3-carboxylate methanol solvate
✍ Scribed by Tang, Qing-Gang ;Wu, Wen-Yuan ;He, Wei ;Sun, Heng-Shun ;Guo, Cheng
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 194 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C~21~H~16~FNO~3~·CH~3~OH, was synthesized by the reaction of 1-naphthol with methyl cyanoacetate and 3-fluorobenzaldehyde in methanol under microwave irradiation. The pyran rings of the two independent molecules in the asymmetric unit adopt boat conformations. The crystal packing is stabilized by intermolecular N—H...O, O—H...O and C—H...π interactions.
📜 SIMILAR VOLUMES
The title compound, C 22 H 18 FNO 3 , was synthesized by the reaction of 1-naphthol with ethyl cyanocaetate and 3-fluorobenzaldehyde in ethanol under microwave irradiation. In the crystal structure, there are intramolecular N-HÁ Á ÁO hydrogen bonds and intermolecular N-HÁ Á ÁO and N-HÁ Á ÁF hydrogen
The title compound, C 22 H 18 FNO 3 , was synthesized by the reaction of 1-naphthol with ethyl cyanocaetate and 4-fluorobenzaldehyde in ethanol under microwave irradiation. The pyran ring adopts a flattened envelope conformation. The molecular conformation and the crystal structure are stabilized by
The title compound, C 23 H 21 NO 4 , was synthesized by the reaction of 1-naphthol with ethyl cyanocaetate and 4methoxybenzaldehyde in ethanol under microwave irradiation. In the structure of C 23 H 21 NO 4 , there are intramolecular and intermolecular N-HÁ Á ÁO hydrogen bonds, also C-HÁ Á Á interac
A view of the molecular structure of (I). The dashed line indicates the intramolecular N-HÁ Á ÁO hydrogen bond. organic papers Acta Cryst. (2005). E61, o3104-o3105 Guo and Gu C 23 H 21 NO 4 o3105