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HRID 11792作成日:2026年10月24日

Aniline → 3-(4-Chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester

https://huagongshe.com/ja/reaction/11792

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物DiisopropylethylamineHCID 81531—
反応物3-(2,4-Dichloro-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044312—
溶媒1-ButanolHCID 263—
溶媒Ethyl AcetateHCID 8857—
生成物3-(4-Chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl esterHCID 21044314—

反応条件

温度100 °C

反応手順

To a solution of 3-(2,4-dichloro-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester (341 mg, 1.0 mmol) (from Example 1d supra) in n-butanol (10 mL) was added aniline (200 mg, 2.15 mmol) (Aldrich) followed by N,N-diisopropylethylamine (258 mg, 2.0 mmol) (Aldrich) and the reaction mixture was heated at 100° C. for 12 hours. After cooling, the reaction mixture was diluted with 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. The crude product was purified by flash column chromatography (silica gel) to give 3-(4-chloro-2-phenylamino-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester. (Yield 45.1 mg, 11.3%).

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-0fc233a13f9f4025aae8312c9520c8fc
出典メモuspto-grants-2006_08