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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1710598Erstellt: 25. Oktober 2026

3-(Difluoromethoxy)benzenesulfonyl chloride → 4-[5-(3-Difluoromethoxy-benzenesulfonylamino)-2-methoxy-phenyl]-piperazine-1-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/1710598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Difluoromethoxy)benzenesulfonyl chlorideHCID 2778226—
EduktTert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylateHCID 10686178—
LösungsmittelPyridineHCID 1049—
Produkt4-[5-(3-Difluoromethoxy-benzenesulfonylamino)-2-methoxy-phenyl]-piperazine-1-carboxylic Acid tert-butyl EsterHCID 5769950675,5%

Reaktionsschritte

0.745 g of 4-(5-Amino-2-methoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (2.423 mmol) were dissolved in 35 ml of pyridine. 0.588 g of 3-(difluoromethoxy)-benzene-sulfonylchloride were added dropwise and the reaction mixture was stirred for 72 h at room temperature. The solvent was evaporated, the residue was dissolved in 40 ml dichloromethane and the organic phase was washed twice with 30 ml aqueous saturated ammonium chloride. The organic phase was dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was purified three times via silica gel chromatography using dichloromethane-methanol, and dichloromethane-ethyl acetate as eluent. 0.94 g of the title compound were isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790727B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-0e696af7ba8c420c99894e94d037ad6f
Quellennotizuspto-grants-2010_09