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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237363Erstellt: 24. Oktober 2026

P-Xylene → N-(3-(3-methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide

https://huagongshe.com/de/reaction/237363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-XyleneHCID 7809—
Edukt3-Methoxy-5-nitroanilineHCID 2759598—
EduktN-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5007601—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-(3-methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5660199642%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (700 mg, 1.92 mmol), 3-methoxy-5-nitroaniline (645 mg, 3.84 mmol) and p-xylene (7 mL) were combined and heated to 140° C., then stirred for 16 hours at 130° C. The reaction was allowed to cool, placed in a sep. funnel, diluted with DCM, and washed with 2M HCl and brine and concentrated in vacuo. The resulting solid was washed with Et2O to give N-(3-(3-methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide (400 mg, 42%). MS (EI) for C21H16N6O7S: 496.94 (MH+)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642584B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-0fad3838e8ef4b1bae977c5c9b738b6e
Quellennotizuspto-grants-2014_02