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Ethyl 2-amino-4-(4-methoxy­phen­yl)-4H-benzo[h]chromene-3-carboxyl­ate

✍ Scribed by Guo, Cheng ;Gu, Xi-feng


Publisher
International Union of Crystallography
Year
2005
Tongue
English
Weight
199 KB
Volume
61
Category
Article
ISSN
1600-5368

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✦ Synopsis


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 interactions.


📜 SIMILAR VOLUMES


Ethyl 2-amino-4-(2-methoxy­phen­yl)-4H-b
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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

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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 22 H 19 NO 3 , was synthesized by the reaction of 1-naphthol with ethyl cyanoacetate and benzaldehyde in ethanol under microwave irradiation. In the crystal structure, weak intermolecular N-HÁ Á ÁO hydrogen bonds link the molecules into centrosymmetric dimers, which are held to