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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634725Generated: October 26, 2026

4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)7-nitroquinazoline hydrochloride → 7-Amino4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochloride

https://huagongshe.com/reaction/634725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)7-nitroquinazoline hydrochlorideHCID 22625047—
CatalystPalladiumHCID 23938—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product7-Amino4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochlorideHCID 2262508497.5%

Reaction Steps

A mixture of 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-nitroquinazoline hydrochloride (5.3 g, 13 mmol) and 10% palladium-on-charcoal catalyst (1 g) in ethanol (100 ml), 7M ethanolic hydrogen chloride (1.8 ml) and methanol (20 ml) was stirred under hydrogen at 1.7 atmospheres for 75 minutes. The catalyst was removed by filtration through diatomaceous earth and the filter pad thoroughly washed with methylene chloride, methanol and ether and the solvent was removed from the filtrate by evaporation to give 7-amino-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochloride (4.8 g, 97%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-f6b0a6199cb3477297a967c0069218d2
Source noteuspto-grants-2001_02