HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 9-bromomethyl-3-methylbenzo[f]quinazolin-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 135622202 | HCID 135622202 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 9-bromomethyl-3-methylbenzo[f]quinazolin-1(2H)-one | HCID 135400976 | 83% |
Reaction Steps
To a hot solution of 3,9-dimethylbenzo[f]quinazolin-1(2H)-one (4.00 g, 17.9 mmol) in benzene (2000 ml) under nitrogen was added N-bromo-succinimide (4.00 g, 22.5 mmol). The reaction mixture was stirred just below reflux for 30 minutes, then at a gentle reflux for 30 minutes. The resulting suspension was allowed to cool for 2 hours, the solid filtered and dried at 70° C. under reduced pressure to give 9-bromomethyl-3-methylbenzo[f]quinazolin-1(2H)-one (4.32 g, 83% purify by NMR).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855712B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-0e6eae7fee3943c690805ab50892e697 |
| Source note | uspto-grants-2005_02 |