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HRID 1797143作成日:2026年10月25日

2,4-Pentanedione, 3-benzyl- → 4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine

https://huagongshe.com/reaction/1797143

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Pentanedione, 3-benzyl-HCID 97757—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amineHCID 608952—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamineHCID 22174870—

反応条件

温度75 °C

反応手順

A suspension of 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (5.25 g, 25.6 mmol), 3-benzylpentane-2,4-dione (5.0 g, 28.4 mmol), and p-toluenesulfonic acid monohydrate (0.475 g, 2.50 mmol) in dimethylsulfoxide (50 mL) was heated to 75° C. for 20 hours. The reaction mixture was allowed to cool to room temperature, and the suspension was dissolved in methylene chloride (700 mL). The solution was washed three times with water, once with brine, dried (magnesium sulfate), and concentrated to afford a moist solid. The crude product was suspended in ethyl acetate (50 mL), heated to reflux, allowed to cool to room temperature, and filtered (repeated three times). The final product was obtained as a white solid containing 3% dimethylsulfoxide by weight: 8.63 g (90%). 1H NMR (CDCl3) δ 8.84–8.53 (m, 1H), 8.48 (d, J=7.9 Hz, 1H), 7.86–7.91 (m, 1H), 7.46–7.50 (m, 1H), 7.13–7.30 (m, 5H), 6.61 (br s, 1H), 6.40 (br s, 1H), 3.83 (s, 2H), 2.79 (s, 3H), 2.24 (s, 3H) ppm. MS (ESI) m/z 358 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07034031B2
出典データセットuspto-grants-2006_04
ORD IDord-71116ed15812458e923992ef58d88cf5
出典メモuspto-grants-2006_04