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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280562Generated: October 26, 2026

Hydrochloric Acid → 3-(4-Fluoro-2-methoxy-phenoxy)quinoxaline-2-carboxylic acid

https://huagongshe.com/reaction/2280562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium carbonateHCID 10796—
Reactant4-Fluoro-2-methoxyphenolHCID 2737368—
ReactantEthyl 3-Chloroquinoxaline-2-carboxylateHCID 12283436—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(4-Fluoro-2-methoxy-phenoxy)quinoxaline-2-carboxylic acidHCID 8672955790.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 3-chloroquinoxaline-2-carboxylate (300 mg, 1.27 mmol), 4-fluoro-2-methoxy-phenol (289.0 μL, 2.54 mmol) and Cs2CO3 (826.3 mg, 2.54 mmol) in NMP (3.0 mL) was stirred at 100° C. for 3 hours. The reaction mixture was poured into water, the pH was adjusted to pH 6 with 1N HCl and the mixture was extracted with ethyl acetate (3×). The organics were combined, washed with brine, dried over Na2SO4 and evaporated to dryness. Purification by column chromatography using a gradient of MeOH in dichloromethane (0-10%) gave 3-(4-fluoro-2-methoxy-phenoxy)quinoxaline-2-carboxylic acid (360 mg, 90%) as a red oil. ESI-MS m/z calc. 314.07, found 315.1 (M+1)+; Retention time: 1.35 minutes (3 minutes run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139529B2
Source datasetuspto-grants-2015_09
ORD IDord-487d48bfc04f4d33a20d44b36a3af62b
Source noteuspto-grants-2015_09