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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791690Generated: November 3, 2026

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

https://huagongshe.com/reaction/1791690

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 numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-85135f206b204869838501aa1ca971d5
Source noteuspto-grants-2006_07