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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


Eth­yl 2-amino-4-(3-fluoro­phen­yl)-4H-b
✍ Guo, Cheng ;Gu, Xi-Feng ;Zhang, Lian-Di ;Li, Yan 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 203 KB

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

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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

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