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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547166Generated: October 29, 2026

4-Chloro-2-fluoroaniline → 7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochloride

https://huagongshe.com/reaction/547166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluoroanilineHCID 93898—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
SolventIsopropanolHCID 3776—
Product7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochlorideHCID 2247826564%

Reaction Steps

A solution of 7-benzyloxy-4chloro-6-methoxyquinazoline (1.2 g, 4 mmol), (prepared as described for the starting material in Example 1), and 4-chloro-2-fluoroaniline (4441 μl, 4 mmol) in 2-propanol (40 ml) was refluxed for 1.5 hours. After cooling, the precipitate was collected by filtration, washed with 2-propanol then ether and dried under vacuum to give 7-benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline hydrochloride (1.13 g, 64%). m.p. 239-242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042353E1
Source datasetuspto-grants-2011_05
ORD IDord-61ed5682752a4d5884546587cb0f5e83
Source noteuspto-grants-2011_05