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HRID 395624作成日:2026年10月26日

Dimethylformamide → 4-(4-Chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole

https://huagongshe.com/reaction/395624

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物1H-Imidazole, 2-(1-methylethyl)-HCID 123457—
反応物2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 10882967—
溶媒WaterHCID 962—
生成物4-(4-Chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 18174757—

反応条件

温度125 °C

反応手順

A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-isopropylimidazole (661 mg), potassium carbonate (830 mg) and N,N-dimethylformamide (10 ml) was stirred at 120-130° C. for 1 hour. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (10 ml×2). The organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole was obtained as an oil (333 mg, 28%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605629B1
出典データセットuspto-grants-2003_08
ORD IDord-272344a9f1f0468898b6c4935bfa6305
出典メモuspto-grants-2003_08