Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737504Generated: October 31, 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/1737504

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-benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-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 numberUS05962458
Source datasetuspto-grants-1999_10
ORD IDord-a9bbf5c6d75b4bbba25ff48b1135fabf
Source noteuspto-grants-1999_10