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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379140Generated: October 26, 2026

Methanol → 6-Amino-4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinoline-3-carbonitrile

https://huagongshe.com/reaction/379140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(3-Chloro-4-fluoro-phenylamino)-7-methoxy-6-nitro-quinoline-3-carbonitrileHCID 10894042—
CatalystIronHCID 23925—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product6-Amino-4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinoline-3-carbonitrileHCID 1114243675.9%

Reaction Steps

A mixture of 4.88 g (13 mmol) of 4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-6-nitro-quinoline-3-carbonitrile, 5.2 g (97.5 mmol) of ammonium chloride, and 3.3 g (58.5 mmol) iron was stirred at reflux in 60 ml of water and 60 ml of methanol for 4.5 hours. The mixture was diluted with 500 ml of hot ethyl acetate and the hot mixture was filtered. The filtration was washed with saturated sodium chloride solution and then the organic layer was dried over sodium sulfate. The solvent was removed and the residue was chromatographed on silica gel eluting with mixture of ethyl acetate and methanol to give 3.38 g of yellow solid: mass spectrum (electrospray, m/e): M+H 343.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297258B1
Source datasetuspto-grants-2001_10
ORD IDord-67d919f5688c4d61800a210d38673189
Source noteuspto-grants-2001_10