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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77429생성일: 2026년 10월 23일

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

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

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참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Benzyl chloroformateHCID 10387—
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl 4-(4-amino-2,6-difluorophenyl)piperazine-1-carboxylateHCID 45925741—
용매WaterHCID 962—
생성물1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazineHCID 2146261790%

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온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841306B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-30f02fab636b452cb88bf9d04bc20bcf
출처 메모uspto-grants-2014_09