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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1800393Erstellt: 27. Oktober 2026

Water → Ethyl ({[5-(3-{[3-(trifluoromethyl)benzoyl]amino}phenoxy)pyridin-2-yl]amino}carbonothioyl)carbamate

https://huagongshe.com/reaction/1800393

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl isothiocyanatoformateHCID 85320—
EduktN-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-3-(trifluoromethyl)benzamideHCID 68419251—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktEthyl ({[5-(3-{[3-(trifluoromethyl)benzoyl]amino}phenoxy)pyridin-2-yl]amino}carbonothioyl)carbamateHCID 8663198459,7%

Reaktionsschritte

To a solution of N-{3-[(6-aminopyridin-3-yl)oxy]phenyl}-3-(trifluoromethyl)benzamide (600 mg, 1.61 mmol) in dimethyl sulfoxide (30 mL) was added ethoxycarbonyl isothiocyanate (230 μL, 1.95 mmol), and the mixture was stirred at room temperature for 12 hr. Water (150 mL) was slowly added to the reaction mixture, and the mixture was extracted with ethyl acetate (300 mL). The organic layer was washed with water (100 mL) and saturated brine (100 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give ethyl ({[5-(3-{[3-(trifluoromethyl)benzoyl]amino}phenoxy)pyridin-2-yl]amino}carbonothioyl)carbamate (485 mg, 59%) as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08344135B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-4d084ace6cd34a00a06653cddbdad458
Quellennotizuspto-grants-2013_01