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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838531Generated: October 26, 2026

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

https://huagongshe.com/reaction/1838531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochlorideHCID 22478265—
SolventTrifluoroacetic acidHCID 6422—
Product7-Hydroxy-6-methoxyquinazolineHCID 136007872130.6%

Reaction Steps

A solution of 7-benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline hydrochloride (892 mg, 2 mmol) in TFA (10 ml) was refluxed 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 pH11 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 numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-2fa4648ac1fe4852b57c1502197c046c
Source noteuspto-grants-2004_01