HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → 4-[(3-Bromophenyl)amino]-6-methylcarbonyloxy-7-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 6-Acetoxy-7-methoxy-3H-quinazolin-4-one | HCID 135681960 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 4-[(3-Bromophenyl)amino]-6-methylcarbonyloxy-7-methoxyquinazoline | HCID 18762901 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of 6-acetoxy-7-methoxy-quinazolin-4-one (RO0505111-000) (1.0 g, 4.26 mmol) (from Example 15, Step A, supra) in SOCl2 (12.5 mL) (Aldrich) was added a few drops of DMF (0.1 mL). The reaction mixture was then heated with stirring at 100° C. for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (20 mL), then 3-bromoaniline (0.806 g, 4.69 mmol) (Aldrich) was added. The reaction mixture was heated at 110° C. for 3 hours. The reaction mixture was cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give 6-acetoxy-4-(3-bromo-phenylamino)-7-methoxy-quinazoline as a gray solid. (Yield 1.65 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217717B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-5e250f1ab4744aa79e3ab2996e8b95c6 |
| Source note | uspto-grants-2007_05 |