HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-(Benzyloxy)-4-(methylsulfanyl)quinazoline → 7-Hydroxy4-methylsulphanylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-(Benzyloxy)-4-(methylsulfanyl)quinazoline | HCID 22649309 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 7-Hydroxy4-methylsulphanylquinazoline | HCID 135674019 | 98.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294532B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-3ba3122f918e4cd69a863aac08259482 |
| Source note | uspto-grants-2001_09 |