HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline | HCID 10661998 | — |
| Reactant | 5-Amino-4-fluoro-2-methylphenyl Methoxyformate | HCID 22625046 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxyquinazoline | HCID 22624931 | 83% |
Reaction Steps
A solution of 7-benzyloxy4-chloro-6-methoxyquinazoline (800 mg, 2.6 mmol), (prepared as described for the starting material in Example 4 but with an aqueous work up), and 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (570 mg, 2.89 mmol) in isopropanol (20 ml) was refluxed for 2 hours. After cooling to ambient temperature, the solid was filtered, washed with isopropanol and dried under vacuum to give 7-benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy4-methylanilino)-6-methoxyquinazoline (1.0 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184225B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-1d47c0213ce84d63b202c3a75e512916 |
| Source note | uspto-grants-2001_02 |