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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756796Generated: October 24, 2026

Sodium Carbonate → 3-ethoxycarbonyl-6,7-difluoro-2-[N-ethyl N-(beta-ethoxycarbonylethyl)amino]quinoline

https://huagongshe.com/en/reaction/1756796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthyl N-ethyl-beta-alaninateHCID 90223—
Reactant2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 9795461—
SolventTolueneHCID 1140—
Product3-ethoxycarbonyl-6,7-difluoro-2-[N-ethyl N-(beta-ethoxycarbonylethyl)amino]quinolineHCID 984283792.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

7.8 g of sodium carbonate are added to a solution of 10 g of 2-chloro-3-ethoxycarbonyl-6,7-difluoroquinoline, prepared as described in Application Example 1, and 9.7 g of N-ethyl-N-(b-ethoxycarbonylethyl)amine in 120 cm3 of toluene. The suspension obtained is heated to approximately 90° C. and then stirred for 4 hours at this temperature. The reaction mixture is then cooled to approximately 20° C. and thereafter washed with 3 times 100 cm3 of water. The organic phase is concentrated to dryness under reduced pressure (20 kPa) at approximately 50° C. 13 g of 3-ethoxycarbonyl-6,7-difluoro-2-[N-ethyl-N-(b-ethoxycarbonylethyl)amino]quinoline are obtained in the form of an oil, which is used without further purification for the subsequent steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442070
Source datasetuspto-grants-1995_08
ORD IDord-17311acfc39048cdb36fc053b4c64d82
Source noteuspto-grants-1995_08