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HRID 21699作成日:2026年10月25日

Potassium Hydroxide → 2-(4-Methoxybenzylamino)-4,6-dimethylnicotinamide

https://huagongshe.com/reaction/21699

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物AcetylacetoneHCID 31261—
反応物4-MethoxybenzylamineHCID 75452—
反応物Ethyl 2-(4-methoxybenzylamino)-4,6-dimethylnicotinateHCID 19933377—
反応物Ethyl beta-amino-beta-ethoxyacrylate hydrochlorideHCID 53395434—
溶媒EthanolHCID 702—
生成物2-(4-Methoxybenzylamino)-4,6-dimethylnicotinamideHCID 1993337670%

反応条件

温度22 °C

反応手順

In a three-necked flask containing ethanol (6.12mL) is added ethyl 3-amino-3-ethoxyacrylate hydrochloride(3g, 15.3mmol). The solution is treated with 4-methoxybenzylamine(2mL, 15.3mmol) and the mixture is stirred at 22° C. for 1.5 h. The reaction mixture was heated to 80° C. for 3 h. The reaction is cooled to 22° C. and an ethanolic solution of potassium hydroxide (0.86 g, 15.3 mmol, 25.0 mL of ethanol) is added. Neat 2,4-pentanedione (1.57 mL, 15.3 mmol) is added to the solution dropwise over 15 minutes at room temperature. The reaction mixture is aged at room temperature for 24 hours. During the age the nicotinate precipitates out of the reaction as does KCl. The reaction mixture is concentrated in vacuo. The crude mixture is chromatographed on silica gel to afford a 70% yield of the product, ethyl 2-(4-methoxybenzylamino )-4,6-dimethylnicotinate, 27.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424432
出典データセットuspto-grants-1995_06
ORD IDord-df276dfc5b8f41f39fbda1b70b2c26ca
出典メモuspto-grants-1995_06