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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1035816Erstellt: 26. Oktober 2026

N-(3-Aminophenyl)methanesulfamide → N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamide

https://huagongshe.com/reaction/1035816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(3-Aminophenyl)methanesulfamideHCID 2734262—
Edukt2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazoleHCID 71060395—
LösungsmittelIsopropanolHCID 3776—
ProduktN-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamideHCID 7106044241%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (0.599 g, 2.42 mmol) and commercially available N-(3-aminophenyl)methanesulfonamide 6 (0.451 g, 2.42 mmol) in 2-propanol (20 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-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide 33 (0.393 g, 41% yield) as a solid. MS (ES) m/z 398 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08546400B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-0e61858142e341b083c509176b3d61c6
Quellennotizuspto-grants-2013_10