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HRID 1928547作成日:2026年10月26日

Triethylamine → 1-{4-[2-(2-Fluorophenoxy)ethyl]piperazin-1-yl}-3-(3,4,5-trimethoxyphenyl)propan-1-one hydrochloride

https://huagongshe.com/reaction/1928547

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,4,5-Trimethoxyhydrocinnamic acidHCID 64860—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1-[2-(2-Fluorophenoxy)ethyl]piperazineHCID 762703—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-{4-[2-(2-Fluorophenoxy)ethyl]piperazin-1-yl}-3-(3,4,5-trimethoxyphenyl)propan-1-one hydrochlorideHCID 6729880256.3%

反応手順

To a mixture of 3-(3,4,5-trimethoxyphenyl)propionic acid (0.36 g, 1.5 mmol), HOBt (0.24 g, 1.8 mmol), EDAC.HCl (0.34 g, 1.8 mmol) in DMF (4 mL) was added 1-[2-(2-fluoro-phenoxy)ethyl]piperazine (0.34 g, 1.5 mmol) and triethylamine (0.5 mL, 3.6 mmol). The mixture was then stirred at room temperature for a day, treated with water, and extracted with dichloromethane. The organic layer was washed with water and brine and then concentrated to dryness. The residue was dissolved in ethyl ether and was added with 2N HCl in ether (1 mL). The white solid was filtered and dried under vacuum to give the title compound (408 mg, 52%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08183374B2
出典データセットuspto-grants-2012_05
ORD IDord-6695f11e100e428a9c8dd487a00325d2
出典メモuspto-grants-2012_05