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HRID 563079作成日:2026年10月26日

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

https://huagongshe.com/reaction/563079

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2-PhenylimidazoleHCID 69591—
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)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazoleHCID 18174764—

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-phenylimidazole (432 mg), potassium carbonate (1.38 g) 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 concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole was obtained as an oil (512 mg, 39%) 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US08067453B2
出典データセットuspto-grants-2011_11
ORD IDord-50d7ca600bb34b8f9d8c3af408c69eb7
出典メモuspto-grants-2011_11