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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351215Generated: November 3, 2026

Ammonium Hydroxide → 4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol

https://huagongshe.com/reaction/1351215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetateHCID 21098397—
SolventMethanolHCID 887—
Product4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-olHCID 21098390—

Reaction Steps

To a solution of 6-acetoxy-4-(4-bromo-2-fluoro-phenylamino)-7-methoxy-quinazoline (1.36 g, 3.34 mmol) (from Example 19, Step A, supra) in MeOH (30 mL) was added an aqueous solution of NH4OH (29%, 0.68 mL, 10 mmol). The reaction mixture was stirred at room temperature for 18 hours, then heated at 100° C. for 1.5 hours. The mixture was then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give the desired 4-(4-bromo-2-fluoro-phenylamino)-7-methoxy-quinazolin-6-ol as a gray solid. (Yield 0.93 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-0565a86a420d4024bff72ce310630ba4
Source noteuspto-grants-2007_05