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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596258Generated: November 1, 2026

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

https://huagongshe.com/reaction/1596258

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-benzyloxy4-chloro-6-methoxyquinazoline (2.18 g, 7.25 mmol), (prepared as described for the starting material in Example 4), 3-acetoxy-4-methylaniline (1.32 g, 8 mmol) and isopropanol (50 ml) was stirred and heated at reflux for 1 hour. The mixture was cooled to ambient temperature. The precipitate was collected by filtration, washed with isopropanol and ether to give 4-(3-acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291455B1
Source datasetuspto-grants-2001_09
ORD IDord-2e765a88cad344cfbe24f03caaa68585
Source noteuspto-grants-2001_09