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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756799Generated: October 24, 2026

Water → 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinoline

https://huagongshe.com/en/reaction/1756799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 9795461—
ReactantEthyl 3-(cyclopropylamino)propanoateHCID 13456042—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinolineHCID 1899458565.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

3 g of sodium carbonate are added to a solution of 3.48 g of 2-chloro-3-ethoxycarbonyl-6,7-difluoroquinoline, prepared as described in Application Example 1, and 3 g of N-cyclopropyl-N-(b-ethoxycarbonylethyl)amine in 10 cm3 of toluene. The suspension obtained is heated to reflux and then stirred for 15 hours at this temperature. The reaction mixture is then cooled to approximately 20° C. and 30 cm3 of water and 4.5 cm3 of acetic acid are thereafter added. After settling has taken place, the reaction mixture is separated and washed with twice 10 cm3 of water. The organic phase is concentrated to dryness under reduced pressure (20 kPa) at approximately 50° C. 3.3 g of crude 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(b-ethoxycarbonylethyl)amino]quinoline are obtained in the form of an oil, which is used without further purification for the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442070
Source datasetuspto-grants-1995_08
ORD IDord-b8ce853ca604497faaa22c81f0a662de
Source noteuspto-grants-1995_08