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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393621Generated: October 29, 2026

2-Pentanol → 6,7-Dimethoxy-3-fluoro-4-(4-chloro-2-fluoro-hydroxyanilino)quinoline hydrochloride

https://huagongshe.com/reaction/393621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PentanolHCID 22386—
Reactant5-Amino-2-chloro-4-fluorophenolHCID 158654—
ReactantHCID 11481892HCID 11481892—
Product6,7-Dimethoxy-3-fluoro-4-(4-chloro-2-fluoro-hydroxyanilino)quinoline hydrochlorideHCID 2264665537%

Reaction Steps

4-Chloro-2-fluoro-5-hydroxyaniline (194 mg, 1.2 mmol), (as described in EP 61741 A2), was added to a suspension of 4-chloro-6,7-dimethoxy-3-fluoroquinoline (241 mg, 1 mmol) in 2-pentanol (5 ml). After refluxing for 15 hours, the precipitate was collected by filtration, washed with isopropanol and dried under vacuum. The solid was partitioned between ethyl acetate and aqueous sodium hydrogen carbonate. The organic layer was washed with water, brine, dried (MgSO4) and the volatiles were removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol 95/5. The purified product was dissolved in methylene chloride/isopropanol and 5M hydrogen chloride in isopropanol (0.5 ml) was added. After evaporation of the methylene chloride, the precipitate was collected by filtration, washed with isopropanol, followed by ether and dried under vacuum to give 6,7-dimethoxy-3-fluoro-4-(4-chloro-2-fluoro-hydroxyanilino)quinoline hydrochloride (150 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-a101f41bfe874d1ab910a716a498f1cd
Source noteuspto-grants-2004_10