Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420936Generated: November 2, 2026

7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazoline hydrochloride → 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride

https://huagongshe.com/reaction/1420936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazoline hydrochlorideHCID 22624930—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochlorideHCID 13567117999.4%

Reaction Steps

A mixture of 7-benzyloxy4-(2-fluoro-5-methoxycarbonyloxy4-methylanilino)-6-methoxyquinazoline hydrochloride (700 mg, 1.4 mmol) and 10% palladium-on-charcoal (100 mg) in DMF (10 ml), methanol (10 ml) and trichloromethane (10 ml) was stirred under hydrogen at 1 atmosphere pressure for 1 hour. The catalyst was removed by filtration through diatomaceous earth and the solvent was removed by evaporation. The residue was triturated with ether, collected by filtration and dried under vacuum to give 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride (570 mg, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071921
Source datasetuspto-grants-2000_06
ORD IDord-d133eccaee284b8cac297d7f3bd49d44
Source noteuspto-grants-2000_06