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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838581Generated: October 31, 2026

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

https://huagongshe.com/reaction/1838581

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 numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-76ee8b6f01094fc5a978ae06f2a6e080
Source noteuspto-grants-2004_01