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HRID 77429作成日:2026年10月24日

Acetone → 1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazine

https://huagongshe.com/ja/reaction/77429

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Benzyl chloroformateHCID 10387—
反応物Sodium BicarbonateHCID 516892—
反応物tert-Butyl 4-(4-amino-2,6-difluorophenyl)piperazine-1-carboxylateHCID 45925741—
溶媒WaterHCID 962—
生成物1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazineHCID 2146261790%

反応条件

温度0 °C

反応手順

To a solution of 4-(4-amino-2,6-difluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (Intermediate III) (25 g, 0.08 mol), in 1:1 acetone:water (300 mL) was added sodium bicarbonate (15.1 g, 0.18 mol). The resulting solution was cooled to 0° C. and benzyl chloroformate (40 mL, 0.24 mol, 50% solution in toluene) was added dropwise. The reaction mixture was stirred at r.t. and progress of the reaction was monitored by TLC. On completion, solvent was evaporated under reduced pressure and the residue was dissolved in ethyl acetate (500 mL). The organic layer was washed with water (2×50 mL), brine (100 mL), dried over anhydrous sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (silica gel, 2:3 ethyl acetate:Pet. ether) to provide title compound (32 g, 90%) as off white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841306B2
出典データセットuspto-grants-2014_09
ORD IDord-30f02fab636b452cb88bf9d04bc20bcf
出典メモuspto-grants-2014_09