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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875493Generated: November 3, 2026

3-Chloro-4-(3-fluorobenzyloxy)aniline → 6-Bromo-N-{3-chloro-4-[(3-fluorophenyl)methoxy]phenyl}quinazolin-4-amine

https://huagongshe.com/reaction/1875493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
Reactant6-Bromo-4-chloro-quinazolineHCID 16770310—
SolventIsopropanolHCID 3776—
Product6-Bromo-N-{3-chloro-4-[(3-fluorophenyl)methoxy]phenyl}quinazolin-4-amineHCID 2473785686%

Reaction Steps

6-bromo-4-chloro-quinazoline (1.36 g) and 3-chloro-4(m-fluoro-benzyloxy)-aniline (1.42 g) were dissolved into 50 mL of isopropanol. The mixture was reacted under reflux for 3 h, and a lot of yellow solid was deposited. The precipitated solid was filtered, and the filter cake was washed with cold ethanol and dried at 60° C. under vacuum overnight to obtain the 6-bromo-4-aminoquinazoline product (2.20 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309563B2
Source datasetuspto-grants-2012_11
ORD IDord-a3a066f3f6b84220bd4cb6d7e01acfb5
Source noteuspto-grants-2012_11