HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochloride → 7-Hydroxy-6-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Benzyloxy-4-(4-chloro-2-fluorophenylamino)-6-methoxyquinazoline hydrochloride | HCID 22478265 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 7-Hydroxy-6-methoxyquinazoline | HCID 136007872 | 130.6% |
Reaction Steps
A solution of 7-benzyloxy-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline hydrochloride (892 mg, 2 mmol) in TFA (10 ml) was refluxed for 50 minutes. After cooling, the mixture was poured onto ice. The precipitate was collected by filtration, dissolved in methanol (10 ml) and basified to pH11 with aqueous ammonia. After concentration by evaporation, the solid product was collected by filtration, washed with water then ether and dried under vacuum to give 4-4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline as a yellow solid (460 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673803B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-2fa4648ac1fe4852b57c1502197c046c |
| Source note | uspto-grants-2004_01 |