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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279575Generated: October 27, 2026

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

https://huagongshe.com/reaction/279575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazolineHCID 21874825—
SolventTolueneHCID 1140—
SolventTrifluoroacetic acidHCID 6422—
Product4-(4-Chloro-2-fluorophenoxy)-7-hydroxy-6-methoxyquinazolineHCID 13561620490.7%

Reaction Steps

A solution of 7-benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (451 mg, 1.1 mmol) in TFA (4.5 ml) was heated at reflux for 3 hours. The mixture was diluted with toluene and the volatiles removed by evaporation. The residue was triturated with methylene chloride, collected by filtration, washed with ether and dried under vacuum to give 4-(4-chloro-2-fluorophenoxy)-7-hydroxy-6-methoxyquinazoline (320 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362336B1
Source datasetuspto-grants-2002_03
ORD IDord-f3d16cce87804cc19f9b2c368fe7fa84
Source noteuspto-grants-2002_03