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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384539Generated: October 29, 2026

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

https://huagongshe.com/reaction/1384539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluoroanilineHCID 93898—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochlorideHCID 22030836—
SolventIsopropanolHCID 3776—
Product7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochlorideHCID 2247826564%

Reaction Steps

A solution of 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (1.34 g, 4 mmol), (prepared as described for the starting material in Example 1), and 4-chloro-2-fluoroaniline (444 μl, 4 mmol) in isopropanol (40 ml ) was refluxed for 1.5 hours. After cooling, the precipitate was collected by filtration, washed with isopropanol 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. 1H NMR Spectrum: (DMSOd6) 4.0(s, 3H); 5.36(s, 2H); 7.39-7.52(m, 9H); 8.1(s, 1H); 8.75(s, 1H) MS-ESI: 410 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-86fc1329af5b47a3abdec69633320bb9
Source noteuspto-grants-2001_07