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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634716Generated: October 30, 2026

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazoline

https://huagongshe.com/reaction/634716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
Reactant5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 22625046—
SolventIsopropanolHCID 3776—
Product7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazolineHCID 2262493183%

Reaction Steps

A solution of 7-benzyloxy4-chloro-6-methoxyquinazoline (800 mg, 2.6 mmol), (prepared as described for the starting material in Example 4 but with an aqueous work up), and 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (570 mg, 2.89 mmol) in isopropanol (20 ml) was refluxed for 2 hours. After cooling to ambient temperature, the solid was filtered, washed with isopropanol and dried under vacuum to give 7-benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy4-methylanilino)-6-methoxyquinazoline (1.0 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-1d47c0213ce84d63b202c3a75e512916
Source noteuspto-grants-2001_02