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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277699Generated: October 30, 2026

N-bromobutanimide → 9-bromomethyl-3-methylbenzo[f]quinazolin-1(2H)-one

https://huagongshe.com/reaction/277699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 135622202HCID 135622202—
SolventBenzeneHCID 241—
Product9-bromomethyl-3-methylbenzo[f]quinazolin-1(2H)-oneHCID 13540097683%

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% purity by NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358952B1
Source datasetuspto-grants-2002_03
ORD IDord-ff8dce9db85c4524ac1e3b73d14811a3
Source noteuspto-grants-2002_03