HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-4-fluoro-2-methylphenyl Methoxyformate → 7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-4-fluoro-2-methylphenyl Methoxyformate | HCID 22625046 | — |
| Reactant | 7-Benzyloxy4-chloroquinazoline hydrochloride | HCID 22625083 | — |
| Solvent | 2-Pentanol | HCID 22386 | — |
| Product | 7-Benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochloride | HCID 22624960 | 97% |
Reaction Steps
2-Fluoro-5-methoxycarbonyloxy-4-methylaniline (883 mg, 4.4 mmol), (prepared as described for the starting material in Example 12), was added to a solution of 7-benzyloxy-4-chloroquinazoline hydrochloride(1 g, 3.7 mmol) in 2-pentanol (15 ml) at 120° C. and the mixture was then heated at reflux for 4 hours. The mixture was allowed to cool and the precipitate was collected by filtration, washed with isopropanol followed by ether and dried under vacuum to give 7-benzyloxy-4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)quinazoline hydrochloride (1.65 g, 97%) as a cream solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362336B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-c55e61c3c6e04642876c8b54030bf043 |
| Source note | uspto-grants-2002_03 |