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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346561Generated: October 26, 2026

7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochloride → 4-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazoline

https://huagongshe.com/reaction/346561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochlorideHCID 22478265—
SolventTrifluoroacetic acidHCID 6422—
Product4-(4-Chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazolineHCID 13551372072%

Reaction Steps

A solution of 7-benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline hydrochloride (892 mg, 2 mmol) in TFA (10 ml) was heated at reflux for 50 minutes. After cooling, the mixture was poured onto ice. The precipitate was collected by filtration, dissolved in methanol (10 ml) and basified to pH 11 with aqueous ammonia. After concentration by evaporation, the solid product was collected by filtration, washed with water then ether and dried under vacuum to give 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline as a yellow solid (460 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173038B1
Source datasetuspto-grants-2007_02
ORD IDord-5e1982cb11a246ffa1eba9f9596fec8d
Source noteuspto-grants-2007_02