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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1073272Erstellt: 26. Oktober 2026

Sodium Hydroxide → 3-Amino-6-fluoro-2-(4-chlorophenyl)-4-quinolinecarboxylic acid

https://huagongshe.com/reaction/1073272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt5-FluoroisatinHCID 236566—
Edukt2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochlorideHCID 2798211—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Amino-6-fluoro-2-(4-chlorophenyl)-4-quinolinecarboxylic acidHCID 1508596995,3%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a stirred suspension of 7 g of 5-fluoroisatin in 58 ml of water was added a solution of 9.36 g of sodium hydroxide in 33 ml of water. The solution was heated to 85° C. and a solution of 12 g of 2-amino-1-(4-chlorophenyl)ethanone hydrochloride in a mixture of 92 ml of ethanol and 40 ml of tetrahydrofuran and 92 ml of water was added drop-wise over 2 hours. After the addition was complete, the solution was refluxed for an additional 30 minutes and then the ethanol and tetrahydrofuran were removed by distillation. The mixture was cooled to 20° C. and filtered through celite. The filtrate was acidified to pH 4 with acetic acid. The solid was filtered off, washed with water and dried, giving 12.8 g of the desired compound as a yellow solid, mp 241°-243° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04968702
Quelldatensatzuspto-grants-1990_11
ORD IDord-5dcee6d70101433ebcaa9e230850c4b0
Quellennotizuspto-grants-1990_11