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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393645Generated: October 29, 2026

4-Chloro-2-fluoroaniline → 7-Benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinoline hydrochloride

https://huagongshe.com/reaction/393645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluoroanilineHCID 93898—
Reactant7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochlorideHCID 22646561—
SolventCyclohexaneHCID 8078—
Product7-Benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinoline hydrochlorideHCID 2264659921%

Reaction Steps

A mixture of 7-benzyloxy-4-chloro-6-methoxyquinoline hydrochloride (300 mg, 0.89 mmol), (prepared as described for the starting material in Example 3), and 4-chloro-2-fluoroaniline (160 mg, 1.1 mmol) was heated at reflux in cyclohexane (20 ml) for 24 hours. The solvent was removed by evaporation and the residue was triturated with ether. The solid crude product was collected by filtration and purified by column chromatography eluting with methylene chloride/methanol (100/0 increasing to 95/5) to give 7-benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinoline hydrochloride (83 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-bccfd38920fb4804ae64bc79f0f9d1f2
Source noteuspto-grants-2004_10