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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073272Generated: October 26, 2026

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

https://huagongshe.com/reaction/1073272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-FluoroisatinHCID 236566—
Reactant2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochlorideHCID 2798211—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-6-fluoro-2-(4-chlorophenyl)-4-quinolinecarboxylic acidHCID 1508596995.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968702
Source datasetuspto-grants-1990_11
ORD IDord-5dcee6d70101433ebcaa9e230850c4b0
Source noteuspto-grants-1990_11