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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165602Generated: October 26, 2026

Iodoethane → Ethyl 7-chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate

https://huagongshe.com/reaction/2165602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 7-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 3018009—
SolventDimethylformamideHCID 6228—
ProductEthyl 7-chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylateHCID 12733855—

Reaction Steps

A 59.7 g portion of the above ester was suspended in 425 ml of dimethylformamide, 76.6 g of potassium carbonate was added and this mixture was stirred in an oil bath at 80°-90° C. An 89 ml portion of ethyl iodide was added, the mixture was stirred at 80°-90° C. for 18 hours and then evaporated. The residue was dissolved in water and then extracted with dichloromethane. The extract was washed with water, dried, filtered through hydrous magnesium silicate and evaporated in vacuo. The solid was recrystallized from ethanol, giving 38 g of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940710
Source datasetuspto-grants-1990_07
ORD IDord-15e1e93cd61741488a0d9eba8c2975d7
Source noteuspto-grants-1990_07