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HRID 38768作成日:2026年10月25日

Dichloromethane → 4-{[2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine

https://huagongshe.com/reaction/38768

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物MorpholineHCID 8083—
反応物TriethylamineHCID 8471—
反応物2-Chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chlorideHCID 2736708—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-{[2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholineHCID 58168707—

反応条件

温度-70 °C

反応手順

A mixture of 2-chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chloride (2.8 g) and dichloromethane (56 mL) was cooled in a dry ice-acetone bath, and morpholine (990 μL) and triethylamine (1.9 mL) were added dropwise thereto while keeping the temperature at −50° C. or lower. The reaction mixture was stirred at −70° C. for 2.5 hours, and then ethyl acetate and water were added thereto. The aqueous layer was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine. After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain 4-{[2-chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine (2.8 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524727B2
出典データセットuspto-grants-2013_09
ORD IDord-67953608ec5b4129a0de88b6f59f7c5b
出典メモuspto-grants-2013_09