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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488967Generated: October 26, 2026

Hydrochloric Acid → 6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1488967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Fluoro-7-nitro-1,4-dihydroquinoxaline-2,3-dioneHCID 9991230—
ReactantHCID 178418642HCID 178418642—
SolventDimethyl SulfoxideHCID 679—
Product6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dioneHCID 986112962.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

First, 9.007 g of 7-fluoro-6-nitro-1,4-dihydroquinoxaline-2,3-dione, 7.611 g of 4-hydroxypyridine, and 5.219 g of powdered potassium hydroxide were added to 120 ml of dry dimethylsulfoxide. The mixture was stirred at 130° C. for 2 hours in a nitrogen atmosphere. Then, 50 ml of ice water and 30 ml of 4N hydrochloric acid were added to the reaction mixture so as to make it weakly acidic (pH 3 to 4). The resultant yellow precipitate was filtered and washed with water. The precipitate was dissolved by heating in a mixture containing 560 ml of water and 56 ml of conc. aqueous ammonia. One gram of activated carbon was added to the resultant mixture, stirred, and filtered. The filtrate was neutralized with conc. hydrochloric acid and ice-cooled. The precipitated crystals were then filtered and washed with water, methanol, and ethanol, successively. The resultant crystals were dried to give 7.56 g of 6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dione (hereinafter, abbreviated as Ia).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677305
Source datasetuspto-grants-1997_10
ORD IDord-08ff0463da474729a90d3320dd332b50
Source noteuspto-grants-1997_10