Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948974Generated: October 30, 2026

Ammonia → 4-((3-Chloro-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol

https://huagongshe.com/reaction/1948974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-((3-Chloro-2-fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetate hydrochlorideHCID 57476866—
SolventMethanolHCID 887—
Product4-((3-Chloro-2-fluorophenyl)amino)-7-methoxyquinazolin-6-olHCID 5747686877.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

6-Acetoxy-4-(3-chloro-2-fluoroanilino)-7-methoxyquinazoline hydrochloride (Reference Example 1, 8.72 g, 21.9 mmol) was dissolved in methanol (200 ml). Concentrated aqueous ammonia (15 ml) was added, and the solution heated to 50° C. with stiffing for 2 hours, causing precipitation of a cream coloured solid. The solid was collected by filtration, washed with diethyl ether (3×200 ml), and dried in vacuo at 60° C. over diphosphorous pentoxide, giving the product as an off white solid (5.40 g, 77%); 1H NMR: 3.95 (s, 3H), 7.19 (s, 1H), 7.23 (dd, 1H), 7.42 (dd, 1H), 7.50 (dd, 1H), 7.64 (s, 1H), 8.32 (s, 1H), 9.43 (s, 1H), 9.67 (br.s, 1H); Mass Spectrum: 320.4, 322.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399667B2
Source datasetuspto-grants-2013_03
ORD IDord-d8084976db2543be9ab116226952cb2e
Source noteuspto-grants-2013_03