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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597239Generated: October 30, 2026

7-(Benzyloxy)-4-(methylsulfanyl)quinazoline → 7-Hydroxy4-methylsulphanylquinazoline

https://huagongshe.com/reaction/1597239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(Benzyloxy)-4-(methylsulfanyl)quinazolineHCID 22649309—
SolventTrifluoroacetic acidHCID 6422—
Product7-Hydroxy4-methylsulphanylquinazolineHCID 13567401998.1%

Reaction Steps

A solution of 7-benzyloxy4-methylsulphanylquinazoline (3 g, 10.6 mmol) in TFA (30 ml) was heated at reflux for 5 hours. After cooling, the volatiles were removed by evaporation. The residue was suspended in water and solid sodium hydrogen carbonate was added until complete dissolution. After extraction with ether, the aqueous layer was acidified to pH2 with 2M hydrochloric acid. The precipitate was collected by filtration, washed with water, followed by ether and dried under vacuum to give 7-hydroxy4-methylsulphanylquinazoline (2 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294532B1
Source datasetuspto-grants-2001_09
ORD IDord-3ba3122f918e4cd69a863aac08259482
Source noteuspto-grants-2001_09