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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 537872Erstellt: 23. Oktober 2026

N-(3-Amino-phenyl)-C,C,C-trifluoro-methanesulfonamide → N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1,1,1-trifluoromethane sulfonamide

https://huagongshe.com/de/reaction/537872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(3-Amino-phenyl)-C,C,C-trifluoro-methanesulfonamideHCID 21757535—
Edukt4-(2-Chlorooxazol-5-yl)benzonitrileHCID 68443558—
LösungsmittelIsopropanolHCID 3776—
ProduktN-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1,1,1-trifluoromethane sulfonamideHCID 7106023276%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.30 g, 1.47 mmol) and N-(3-aminophenyl)-1,1,1-trifluoromethanesulfonamide 43 (0.35 g, 1.45 mmol) in 2-propanol (25 mL) was heated to 80° C. for 14 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1,1,1-trifluoromethane sulfonamide 44 (0.45 g, 75% yield) as a solid. MS (ES) m/z 409 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865709B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-3626c877453a46bcbf016d2357f3a0ab
Quellennotizuspto-grants-2014_10