HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetate | HCID 21098397 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-((4-Bromo-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol | HCID 21098390 | — |
Reaction Steps
To a solution of 6-acetoxy-4-(4-bromo-2-fluoro-phenylamino)-7-methoxy-quinazoline (1.36 g, 3.34 mmol) (from Example 19, Step A, supra) in MeOH (30 mL) was added an aqueous solution of NH4OH (29%, 0.68 mL, 10 mmol). The reaction mixture was stirred at room temperature for 18 hours, then heated at 100° C. for 1.5 hours. The mixture was then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give the desired 4-(4-bromo-2-fluoro-phenylamino)-7-methoxy-quinazolin-6-ol as a gray solid. (Yield 0.93 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217717B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-0565a86a420d4024bff72ce310630ba4 |
| Source note | uspto-grants-2007_05 |