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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737537Generated: October 31, 2026

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

https://huagongshe.com/reaction/1737537

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluorophenolHCID 181975—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochlorideHCID 22030836—
SolventPyridineHCID 1049—
Product7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazolineHCID 2187482577%

Reaction Steps

4-Chloro-2-fluoro-phenol (264 mg, 1.8 mmol) was added to a solution of 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (506 mg, 1.5 mmol), (prepared as described for the starting material in Example 1), in pyridine (8 ml) and the mixture heated at reflux for 45 minutes. The solvent was removed by evaporation and the residue partitioned between ethyl acetate and water. The organic layer was washed with 0.1M hydrochloric acid, water and brine, dried (MgSO4) and the solvent removed by evaporation. The solid residue was triturated with petroleum ether and the crude product collected by filtration and purified by flash chromatography eluting with methylene chloride/ether (9/1) to give 7-benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (474 mg, 77%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962458
Source datasetuspto-grants-1999_10
ORD IDord-4188eb714b6846fc93731af2f6b4ca84
Source noteuspto-grants-1999_10