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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655619Erstellt: 25. Oktober 2026

Potassium Carbonate → N-(3-chloroquinoxalin-2-yl)-3-fluorobenzenesulfonamide

https://huagongshe.com/reaction/655619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2,3-DichloroquinoxalineHCID 16659—
Edukt3-FluorobenzenesulfonamideHCID 150924—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(3-chloroquinoxalin-2-yl)-3-fluorobenzenesulfonamideHCID 5762536584,6%

Reaktionsbedingungen

Temperatur135 °C

Reaktionsschritte

3-fluorobenzenesulfonamide (250 mg, 1.4 mmol), 2,3-dichloroquinoxaline (284.1 mg, 1.4 mmol) and dry K2CO3 (198.4 mg, 1.4 mmol) are dissolved in dry DMF (0.8 ml) and heated up to 135° C. in a sealed tube for 2.5 h. When TLC confirms the completion of the reaction, the reaction mixture is cooled down to rt and quenched by addition of water (4 ml) and AcOH (0.03 ml). The residue obtained is triturated and the resulting solid is filtered and washed with water until neutral pH then dried under vacuum to afford 400 mg (83%) of the title compound as an off white solid. 1H NMR (DMSO-d6) δ 12.8-10.9 (br s, 1H), 8.05-7.62 (m, 7H), 7.54 (td, J=2.0, 8.5 Hz, 1H). HPLC (max plot) 94%; Rt 3.79 min. LC/MS: (ES+): 338.1, (ES−): 336.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071597B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-54ce079d10104fa0ad01baa3cd563bda
Quellennotizuspto-grants-2011_12