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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77429Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
Edukttert-Butyl 4-(4-amino-2,6-difluorophenyl)piperazine-1-carboxylateHCID 45925741—
LösungsmittelWaterHCID 962—
Produkt1-(Tert-butoxycarbonyl)-4-[2,6-difluoro-4-(benzyloxycarbonyl)aminophenyl]piperazineHCID 2146261790%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841306B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-30f02fab636b452cb88bf9d04bc20bcf
Quellennotizuspto-grants-2014_09