HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 4-(3-Acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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-benzyloxy4-chloro-6-methoxyquinazoline (2.18 g, 7.25 mmol), (prepared as described for the starting material in Example 4), 3-acetoxy-4-methylaniline (1.32 g, 8 mmol) and isopropanol (50 ml) was stirred and heated at reflux for 1 hour. The mixture was cooled to ambient temperature. The precipitate was collected by filtration, washed with isopropanol and ether to give 4-(3-acetoxy-4-methylanilino)-7-benzyloxy-6-methoxyquinazoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06291455B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-2e765a88cad344cfbe24f03caaa68585 |
| Source note | uspto-grants-2001_09 |