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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612159Generated: October 27, 2026

Sodium Carbonate → 4-(4-Chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrile

https://huagongshe.com/reaction/612159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium HydroxideHCID 14923—
Reactant5-Amino-2-chloro-4-fluorophenolHCID 158654—
ReactantMethylcarbonateHCID 4585885—
Reactant1-EthoxyethanolHCID 10129898—
Reactant4-Chloro-6,7,8-trimethoxy-3-quinolinecarbonitrileHCID 22466611—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-(4-Chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrileHCID 22466624—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 0.279 g of 4-chloro-6,7,8-trimethoxy-3-quinolinecarbonitrile, 0.22 g of the methyl carbonate of 4-chloro-2-fluoro-5-hydroxy-aniline, and 15 ml of ethoxy-ethanol was stirred under nitrogen, at reflux temperature for 30 minutes. The mixture was cooled and added to 100 ml of water. To this mixture was added sodium carbonate to pH 9. The product was collected, washed with water, and dried. The solids thus obtained were dissolved in a mixture of 30 ml of methyl alcohol and 20 ml of acetone. To this mixture was added 1.5 ml of 28-30% ammonium hydroxide solution. The mixture was heated at 50° C. for 30 minutes and concentrated. The product was collected, washed with ethyl acetate, and dried to give 0.162 g of 4-(4-chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrile as a solid, mp 223-225° C.; mass spectrum (EI, m/e): M 403.0731.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-9b0f59a9c5224ce9a4ece0e856e5b7b3
Source noteuspto-grants-1999_12