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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248457Generated: October 25, 2026

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

https://huagongshe.com/reaction/248457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCarbonate IonHCID 19660—
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 pctassium 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 numberUS05210193
Source datasetuspto-grants-1993_05
ORD IDord-6c7f721e79ef4d0ea1647af4db81e93b
Source noteuspto-grants-1993_05