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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068589Erstellt: 26. Oktober 2026

Diethyl Oxalate → 6,7-Difluoroquinoxaline-2,3(1H,4H)-dione

https://huagongshe.com/reaction/1068589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
Produkt6,7-Difluoroquinoxaline-2,3(1H,4H)-dioneHCID 822839—

Reaktionsschritte

The title compound (Sarges, R. et al., J. Med. Chem. 33.2240 (1990)) was prepared using an adaptation of the method of Cheeseman. (Cheeseman, G. W. H. J. Cam. Soc. 1171 (1962)). A mixture of diethyl oxalate (1.11 g, 7.63 mmol and 4,5-difluoro-1,2-diaminobenzene (110 mg, 0.763 mmol) was heated to reflux under N2 for 2 h. The reaction was allowed to cool to room temperature and the solid was collected by vacuum filtration, rinsed with hexanes, and air dried. This gray brown solid was recrystallized from 20 mL of EtOH and the brown-white crystals collected by vacuum filtration and the crystals further dried under vacuum (0.5 torr, 25° C.) to yield 45.3 mg (30.0%); mp >360° C. (lit. >310° C.); 1H NMR (d6-acetone) δ 7.19 (t, 2H, ArH, JH-F=9.3), 10.9 (br s, 2H, NH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06251903B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-f3301b631ce841988542bc08c9a97de0
Quellennotizuspto-grants-2001_06