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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600702Generated: October 31, 2026

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

https://huagongshe.com/reaction/1600702

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 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977107
Source datasetuspto-grants-1999_11
ORD IDord-349542d2a6864f8b8f9dd9cedfef6abb
Source noteuspto-grants-1999_11