Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384530Generated: October 28, 2026

7-Benzyloxy-6-methoxy-4-phenoxyquinazoline → 7-Hydroxy-6-methoxy-4-phenoxyquinazoline

https://huagongshe.com/reaction/1384530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-6-methoxy-4-phenoxyquinazolineHCID 21874814—
SolventTrifluoroacetic acidHCID 6422—
Product7-Hydroxy-6-methoxy-4-phenoxyquinazolineHCID 13549613789%

Reaction Steps

7-Benzyloxy-6-methoxy-4-phenoxyquinazoline (160 mg, 0.44 mmol) in TFA (3 ml) was heated at reflux for 30 minutes. The solvent was removed by evaporation and the residue treated with aqueous sodium hydrogen carbonate solution. The precipitated product was collected by filtration, washed with water and dried to give 7-hydroxy-6-methoxy-4-phenoxyquinazoline (105 mg, 88%). 1H NMR Spectrum: (DMSOd6) 4.00(s, 3H); 7.20(s, 1H); 7.25-7.35(m, 3H); 7.4-7.55(m, 2H); 7.58(s, 1H); 10.73(s, 1H) MS-ESI: 269 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-fb6eb260f83b4e3da7287ee993d35058
Source noteuspto-grants-2001_07