HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182523Generated: November 2, 2026
7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline
https://huagongshe.com/reaction/2182523
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline | HCID 10661998 | — |
| Reactant | 3-Acetoxy-4-methylaniline | HCID 22478311 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline | HCID 22478289 | — |
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-33b9ed28e8c94f23a1c756e9c7b8702b |
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| Source note | uspto-grants-2005_05 |
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