HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 4-(4-Chloro-2,6-difluoroanilino)-6,7-dimethoxyquinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Chloro-2,6-difluoroaniline hydrochloride | HCID 21260280 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinazoline hydrochloride | HCID 22022161 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(4-Chloro-2,6-difluoroanilino)-6,7-dimethoxyquinazoline hydrochloride | HCID 21260346 | 16% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinazoline hydrochloride (210 mg, 0.8 mmol), (prepared as described for the starting material in Example 1 but without the aqueous work up), and 4-chloro-2,6-difluoroaniline hydrochloride (177 mg, 0.89 mmol) in isopropanol (8 ml) were heated at reflux for 2 hours. The reaction mixture was then allowed to cool, hexane added and the precipitated product collected by filtration, washed with isopropanol and dried to give 4-(4-chloro-2,6-difluoroanilino)-6,7-dimethoxyquinazoline hydrochloride (45 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184225B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-1c08663b789746239cd3db8c214771a6 |
| Source note | uspto-grants-2001_02 |