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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1756799Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 9795461—
EduktEthyl 3-(cyclopropylamino)propanoateHCID 13456042—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelTolueneHCID 1140—
Produkt3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinolineHCID 1899458565,6%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05442070
Quelldatensatzuspto-grants-1995_08
ORD IDord-b8ce853ca604497faaa22c81f0a662de
Quellennotizuspto-grants-1995_08