関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Acetylacetone | HCID 31261 | — |
| 反応物 | 4-Methoxybenzylamine | HCID 75452 | — |
| 反応物 | Ethyl 2-(4-methoxybenzylamino)-4,6-dimethylnicotinate | HCID 19933377 | — |
| 反応物 | Ethyl beta-amino-beta-ethoxyacrylate hydrochloride | HCID 53395434 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4-Methoxybenzylamino)-4,6-dimethylnicotinamide | HCID 19933376 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05424432 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-df276dfc5b8f41f39fbda1b70b2c26ca |
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| 出典メモ | uspto-grants-1995_06 |
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