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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712412Generated: October 30, 2026

4-Bromo-2-fluoroaniline → 4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetate

https://huagongshe.com/reaction/712412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-fluoroanilineHCID 123050—
Reactant4-Chloro-7-methoxyquinazolin-6-yl acetateHCID 22022160—
SolventIsopropanolHCID 3776—
Product4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetateHCID 2109839784.5%

Reaction Conditions

Temperature83 °C

Reaction Steps

A suspension of 4-chloro-7-methoxyquinazolin-6-yl acetate (2.05 g), 4-bromo-2-fluoroaniline (2.11 g, 1.30 eq) and isopropanol (40 mL) was stirred at 83° C. overnight. The reaction mixture was cooled to room temperature and filtered, the residue was washed with 100 mL of isopropanol and dried to afford the desired compound as a solid (2.78 g, 84.50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-e5a21b178450487a9a45dc92ca415f40
Source noteuspto-grants-2015_11