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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439442Generated: October 25, 2026

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

https://huagongshe.com/reaction/439442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
Product6,7-Difluoroquinoxaline-2,3(1H,4H)-dioneHCID 822839—

Reaction Steps

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. Chem. 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 collected by vacuum filtration and 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) δ7.19 (t, 2H, ArH, JH-F =9.3), 10.9 (br s, 2H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514680
Source datasetuspto-grants-1996_05
ORD IDord-84e4cc14a18848a7ad2f4a2006205e5e
Source noteuspto-grants-1996_05