Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634743Generated: October 31, 2026

4-Chloro-6-methoxy-7-nitroquinazoline hydrochloride → 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochloride

https://huagongshe.com/reaction/634743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-methoxy-7-nitroquinazoline hydrochlorideHCID 21260306—
Reactant5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 22625046—
SolventIsopropanolHCID 3776—
Product4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochlorideHCID 2126034291.2%

Reaction Steps

A mixture of 4-chloro-6-methoxy-7-nitroquinazoline hydrochloride (784 mg, 2.8 mmol) and 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (621 mg, 3.1 mmol), (prepared as described for the starting material in Example 26), in isopropanol (10 ml) was heated at reflux for 2 hours. The mixture was allowed to cool, the precipitated product collected by filtration, washed with isopropanol, ether and dried under vacuum to give 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochloride (1.12 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-6d95b8789c16449fb7234774c19c7ae2
Source noteuspto-grants-2001_02