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HRID 1396124作成日:2026年10月25日

Ethyl benzoylacetate → Carbamic acid 3-[4-(4-fluoro-phenyl)-piperazin-1-yl]-3-oxo-1-phenyl-propyl ester

https://huagongshe.com/reaction/1396124

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl benzoylacetateHCID 7170—
反応物TetrahydrofuranHCID 8028—
反応物Ammonium HydroxideHCID 14923—
反応物1-(4-Fluorophenyl)piperazineHCID 75260—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Carbamic acid 3-[4-(4-fluoro-phenyl)-piperazin-1-yl]-3-oxo-1-phenyl-propyl esterHCID 25167253—

反応条件

温度0 °C

反応手順

Ethyl benzoylacetate (2.887 mmol) and 4-fluorophenylpiperazine (2.887 mmol) were dissolved in toluene, and refluxed for 24 hours. The resulting reaction mixture was concentrated under a reduced pressure, and dissolved in methanol, and cooled to 0° C., and sodium borohydride (2.887 mmol) was then added dropwise to the resulting mixture. The resulting mixture was stirred at a room temperature for 2 hours, concentrated under a reduced pressure, diluted with water, and then extracted several times with ethyl acetate to obtain an organic phase. The resulting organic phase was dried over magnesium sulfate, filtered, and then concentrated under a reduced pressure. The resulting mixture was purified with column chromatography (hexane:ethyl acetate=1:1) to obtain a compound. The prepared compound was dissolved in tetrahydrofuran (10 mL), and 1,1′-carbodiimidazole (5 mmol) was added to the resulting mixture. Then, the resulting mixture was stirred at a room temperature for 1 hour, and excessive ammonium hydroxide was added to the reaction mixture. The resulting reaction mixture was stirred at a room temperature for 1 hour. The reaction mixture was diluted with water, and extracted several times with ethyl acetate to obtain an organic phase. The prepared organic phase was dried over magnesium sulfate, filtered, and then concentrated under a reduced pressure. The resulting pellet was purified with column chromatography (ethyl acetate) to obtain a title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08901116B2
出典データセットuspto-grants-2014_12
ORD IDord-d372ebc6ef204fdbae1a51f5b0d0894d
出典メモuspto-grants-2014_12