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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393667Generated: October 30, 2026

Sodium Hydroxide → 6-Carboxy-4-(4-chloro-2-fluoroanilino)-7-methoxyquinoline

https://huagongshe.com/reaction/393667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-(4-Chloro-2-fluoroanilino)-7-methoxy-6-methoxycarbonylquinolineHCID 22646570—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Carboxy-4-(4-chloro-2-fluoroanilino)-7-methoxyquinolineHCID 2264662091.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-(4-chloro-2-fluoroanilino)-7-methoxy-6-methoxycarbonylquinoline (1.79 g, 4.9 mmol), (prepared as described in Example 55), and sodium hydroxide (0.6 g, 15 mmol) in methanol (75 ml) and water (5 ml) was heated at 70° C. for 4 hours. The mixture was allowed to cool and the volatiles were removed by evaporation. The solid residue was suspended in water and acetic acid was added to adjust the aqueous suspension to pH5. The mixture was stirred for 15 minutes and the solid product was collected by filtration, washed with water and then acetone and finally ether, and dried to give 6-carboxy-4-(4-chloro-2-fluoroanilino)-7-methoxyquinoline (1.55 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-fb7c19e83af14bb8900343397ae3b7dc
Source noteuspto-grants-2004_10