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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007867Generated: October 31, 2026

Triethylamine → Ethyl 4-ethyl-7-fluoro-6-methoxy-2-oxo-1,2-dihydro-3-quinolinecarboxylate

https://huagongshe.com/reaction/1007867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 10104164HCID 10104164—
Reactant2-Ethylpropanedioyl dichlorideHCID 10920924—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-ethyl-7-fluoro-6-methoxy-2-oxo-1,2-dihydro-3-quinolinecarboxylateHCID 2189200885.3%

Reaction Steps

A solution of ethylmalonyl chloride (12.9 ml, 100 mmol) in anhydrous acetonitrile (30 ml) is added dropwise, under argon and at 0° C. to a solution of 1-(2-amino-4-fluoro-5-methoxyphenyl)-1-propanone (15.3 g, 77.5 mmol) and triethylamine (13.9 ml, 100 mmol) in anhydrous acetonitrile (110 ml). The reaction medium is left to return to ambient temperature, a solution of sodium ethylate (obtained by 1.8 g, 78 mmol of sodium in 80 ml of ethanol) is cannulated dropwise and under argon, then the reaction medium is left under agitation for 12 hours at ambient temperature. The reaction mixture is poured into ice-cooled water (100 ml) and agitation is carried out for two hours, then the precipitate is filtered out and washed with water, with ethanol and with ether. 19.4 g of a white solid is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797715B1
Source datasetuspto-grants-2004_09
ORD IDord-62d32b041ea1483e999e6e9f76797894
Source noteuspto-grants-2004_09