HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6-methoxy-7-nitroquinazoline hydrochloride → 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6-methoxy-7-nitroquinazoline hydrochloride | HCID 21260306 | — |
| Reactant | 5-Amino-4-fluoro-2-methylphenyl Methoxyformate | HCID 22625046 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochloride | HCID 21260342 | 91.2% |
Reaction Steps
A mixture of 4-chloro-6-methoxy-7-nitroquinazoline hydrochloride (784 mg, 2.8 mmol) and 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (621 mg, 3.1 mmol), (prepared as described for the starting material in Example 26), in isopropanol (10 ml) was heated at reflux for 2 hours. The mixture was allowed to cool, the precipitated product collected by filtration, washed with isopropanol, ether and dried under vacuum to give 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-6-methoxy-7-nitroquinazoline hydrochloride (1.12 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184225B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-6d95b8789c16449fb7234774c19c7ae2 |
| Source note | uspto-grants-2001_02 |