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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577357Generated: October 26, 2026

7-Benzyloxy4-(4-bromo-2-fluoroanilino)-6-methoxyquinazoline hydrochloride → 4-[(4-Bromo-2-fluorophenyl)amino]-6-methoxy-7-quinazolinol

https://huagongshe.com/reaction/577357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy4-(4-bromo-2-fluoroanilino)-6-methoxyquinazoline hydrochlorideHCID 18753473—
SolventTrifluoroacetic acidHCID 6422—
Product4-[(4-Bromo-2-fluorophenyl)amino]-6-methoxy-7-quinazolinolHCID 13550385282%

Reaction Steps

A solution of 7-benzyloxy-4-(4-bromo-2-fluoroanilino)-6-methoxyquinazoline hydrochloride (9.4 g, 19.1 mmol) in TFA (90 ml) was heated at reflux for 50 minutes. The mixture was allowed to cool and was poured on to ice. The resulting precipitate was collected by filtration and dissolved in methanol (70 ml). The solution was adjusted to pH9-10 with concentrated aqueous ammonia solution. The mixture was concentrated to half initial volume by evaporation. The resulting precipitate was collected by filtration, washed with water and then ether, and dried under vacuum to give 4-(4-bromo-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (5.66 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040548B2
Source datasetuspto-grants-2015_05
ORD IDord-996e2cbea39b48c2b89c0ced3a5690a1
Source noteuspto-grants-2015_05