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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916458Generated: October 30, 2026

4-Chloro-7-methoxyquinazolin-6-yl acetate → 4-Chloro-7-methoxyquinazolin-6-ol

https://huagongshe.com/reaction/916458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-methoxyquinazolin-6-yl acetateHCID 22022160—
SolventAmmoniaHCID 222—
Product4-Chloro-7-methoxyquinazolin-6-olHCID 2313247567.8%

Reaction Conditions

Temperature10 °C

Reaction Steps

6-Acetoxy-4-chloro-7-methoxyquinazoline (10.0 g, 39.6 mmol), (WO 01/04102, Table VI examples), was added in portions to a stirred 7N methanolic ammonia solution (220 ml) and the mixture cooled to 10° C. in an ice/water bath. Initially the solid dissolved to give a yellow solution which then deposited a yellow precipitate. After stirring for one hour the precipitate was filtered off, washed with diethyl ether and dried thoroughly under high vacuum to give 4-chloro-6-hydroxy-7-methoxyquinazoline (5.65 g, 67.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268230B2
Source datasetuspto-grants-2007_09
ORD IDord-dabbb77dc4ee4de6a88378da173b268a
Source noteuspto-grants-2007_09