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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577381Generated: October 28, 2026

7-Benzyloxy-4-(2-fluoro-4-methylanilino)-6-methoxyquinazoline hydrochloride → HCID 135537648, compound

https://huagongshe.com/reaction/577381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(2-fluoro-4-methylanilino)-6-methoxyquinazoline hydrochlorideHCID 17973220—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 135537648HCID 13553764874%

Reaction Steps

A solution of 7-benzyloxy-4-(2-fluoro-4-methylanilino)-6-methoxyquinazoline hydrochloride (2 g, 4.7 mmol) in TFA (20 ml) was heated at 80° C. for 5 hours and stirred at ambient temperature overnight. The volatiles were removed under vacuum and the residue was suspended in water (50 ml). Solid sodium hydrogen carbonate was added until the pH was approximately 7. The precipitate was then collected by filtration, washed with water and dried under vacuum. The solid was purified by column chromatography eluting with methanol/methylene chloride (5/95). After removal of the solvent by evaporation, the solid was triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 4-(2-fluoro-4-methylanilino)-7-hydroxy-6-methoxyquinazoline (1.04 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040548B2
Source datasetuspto-grants-2015_05
ORD IDord-7018ffbe994245ec8ed06af6d2a97f98
Source noteuspto-grants-2015_05