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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372992Generated: October 30, 2026

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

https://huagongshe.com/reaction/1372992

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-fluorophenylamino)-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 pH 9–10 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-fluorophenylamino)-7-hydroxy-6-methoxyquinazoline (5.66 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160889B2
Source datasetuspto-grants-2007_01
ORD IDord-947a28ab8e42456889a0ea9d616f3db6
Source noteuspto-grants-2007_01