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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747554Generated: November 2, 2026

Urea → HCID 86678205, compound

https://huagongshe.com/reaction/1747554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantPotassium IodideHCID 4875—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86678204HCID 86678204—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 86678205HCID 8667820533%

Reaction Conditions

Temperature0 °C

Reaction Steps

In 2.0 mol/L hydrochloric acid (50.0 mL) was dissolved 3-chloro-2-(2,2,2-trifluoro-1-(pyridin-3-yl)ethoxy) quinoxaline-6-amine (2.00 g, 5.64 mmol) obtained in Step 3 and the mixture was cooled to 0° C. Sodium nitrite (506 mg, 7.33 mmol) was added and the mixture was stirred at 0° C. for 10 minutes. Urea (508 mg, 8.46 mmol) was added to the reaction mixture and the mixture was stirred at 0° C. for 10 minutes. Potassium iodide (2.34 g, 14.1 mmol) dissolved in water (10.0 mL) was slowly added and the mixture was stirred at room temperature for 30 minutes. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were added to the reaction mixture. Extraction with ethyl acetate, washing with saturated brine and drying over anhydrous magnesium sulfate were performed. After filtration, the solvent in the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/0 to 3/2) to give Compound A47 (868 mg, 33% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150569B2
Source datasetuspto-grants-2015_10
ORD IDord-1333e7a69d80476c89e1304416c59ade
Source noteuspto-grants-2015_10