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HRID 11766作成日:2026年10月26日

Aniline → 3-(2,4-Diphenylamino-pyrimidin-5-yl)-2-(2,6-dichloro-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/11766

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物2-(2,6-Dichloro-phenyl)-3-(2,4-dichloro-pyrimidin-5-yl)-propionic acid methyl esterHCID 21044324—
生成物3-(2,4-Diphenylamino-pyrimidin-5-yl)-2-(2,6-dichloro-phenyl)-propionic acid methyl esterHCID 21044327—

反応条件

温度110 °C

反応手順

A mixture of 2-(2,6-dichloro-phenyl)-3-(2,4-dichloro-pyrimidin-5-yl)-propionic acid methyl ester (0.20 g, 0.53 mmol) (from Example 2a supra) and aniline (2.0 ml) (Aldrich) was heated at 110° C. for 2 hours. The reaction mixture was washed with hexanes (50 mL×3) and the supernatant was decanted off after each time. The residue was then dissolved in ethyl acetate (100 mL) and successively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give the crude 3-(2,4-diphenylamino-pyrimidin-5-yl)-2-(2,6-dichloro-phenyl)-propionic acid methyl ester as a brown caramel which was used in the next step without further purification. (Yield 0.18 g, 69.3%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098332B2
出典データセットuspto-grants-2006_08
ORD IDord-a348e451808443f4981f4358045c1ae5
出典メモuspto-grants-2006_08