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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597217Generated: October 31, 2026

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochloride → 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline

https://huagongshe.com/reaction/1597217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochlorideHCID 22030836—
SolventDichloromethaneHCID 6344—
Product7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 1066199897.1%

Reaction Steps

A mixture of 7-benzyloxy-6-methoxy-3,4-dihydroquinazolin-4-one (2.82 g, 0.01 mol), thionyl chloride (40 ml) and DMF (0.28 ml) was stirred and heated at reflux for 1 hour. The mixture was evaporated and azeotroped with toluene to give 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (3.35 g). 7-Benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (3.35 g) was dissolved in methylene chloride (250 ml) and washed with sodium hydrogen carbonate until the aqueous layer was adjusted to pH8. The organic layer was washed with brine, dried (MgSO4) and evaporated to give 7-benzyloxy-4-chloro-6-methoxyquinazoline (2.9 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-82c5b7054800490295b7e7f0151e4519
Source noteuspto-grants-2001_09