HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182524Generated: November 2, 2026
4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline → 4-(3-Acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline
https://huagongshe.com/reaction/2182524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline | HCID 22478289 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline | HCID 135450804 | 107.6% |
Reaction Steps
A mixture of 7-benzyloxy-4-chloro-6-methoxyquinazoline (20.8 g, 7.25 mmol), 3-acetoxy-4-methylaniline (1.32 g, 8 mmol) and 2-propanol (50 ml) was stirred and heated to reflux for 1 hour. The mixture was cooled to ambient temperature. The precipitate was collected by filtration, washed with 2-propanol and ether to give 4-(3-acetoxy-4methylanilino)-7-benzyloxy-6-methoxyquinazoline. A mixture of 4-(3-acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline (2.68 g, 5.75 mmol), 10% palladium-on-charcoal catalyst (0.27 g) in methanol (50 ml), DMF (12 ml) and trichloromethane (50 ml) was stirred at ambient temperature under 1.5 atmospheres of hydrogen for 30 minutes. The catalyst was removed by filtration and the filtrate evaporated. The residual solid was triturated in ether, collected by filtration and dried under vacuum at 50° C. to give 4-(3-acetoxy-4-methylanilino)-7-hydroxy-6-methoxyquinazoline (2.1 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897210B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-3a7092eac16e4252b34701e4a654ffe2 |
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| Source note | uspto-grants-2005_05 |
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