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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182523Generated: November 2, 2026

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline

https://huagongshe.com/reaction/2182523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
Reactant3-Acetoxy-4-methylanilineHCID 22478311—
SolventIsopropanolHCID 3776—
Product4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazolineHCID 22478289—

Reaction Steps

A mixture of 7-benzyloxy-4-chloro-6-methoxyquinazoline (20.8 g, 7.25 mmol), 3-acetoxy-4-methylaniline (1.32 g, 8 mmol) and 2-propanol (50 ml) was stirred and heated to reflux for 1 hour. The mixture was cooled to ambient temperature. The precipitate was collected by filtration, washed with 2-propanol and ether to give 4-(3-acetoxy-4methylanilino)-7-benzyloxy-6-methoxyquinazoline. A mixture of 4-(3-acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline (2.68 g, 5.75 mmol), 10% palladium-on-charcoal catalyst (0.27 g) in methanol (50 ml), DMF (12 ml) and trichloromethane (50 ml) was stirred at ambient temperature under 1.5 atmospheres of hydrogen for 30 minutes. The catalyst was removed by filtration and the filtrate evaporated. The residual solid was triturated in ether, collected by filtration and dried under vacuum at 50° C. to give 4-(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline (2.1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897210B2
Source datasetuspto-grants-2005_05
ORD IDord-33b9ed28e8c94f23a1c756e9c7b8702b
Source noteuspto-grants-2005_05