Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377048Generated: October 31, 2026

Benzoyl Peroxide → HCID 135838176, compound

https://huagongshe.com/reaction/1377048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 135838215HCID 135838215—
SolventBenzeneHCID 241—
ProductHCID 135838176HCID 135838176—

Reaction Steps

To a solution of N-(6-methyl-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamide (1.76 g, 5.7 mmoles) in dry benzene (150 ml) was added N-bromosuccinimide (1.01 g, 5.7 mmoles) and dibenzoyl peroxide (15 mg). The mixture was heated to reflux under a nitrogen atmosphere for 2.5 hours. After cooling, benzene was removed under reduced pressure, and the residue was purified on a silica gel column eluting with chloroform to give N-(6-(bromomethyl)-1,2-dihydro-1-oxobenzo[f]quinazolin-3-yl)pivalamide as an off-white solid. (1.4 g, 57%) 1H NMR (DMSO-d6, 200 MHz) δ: 1.27(s, 9H, t-butyl); 5.26(s, 2H, CH2Br); 7.63-7.81(m, 3H, Ar); 8.26(dd, J=7.6, 2.0 Hz, 1H, Ar); g.81(dd, J=7.8, 2.0 Hz, 1H, Ar); 11.27(s, 1H, NH); 12.33(s, 1H, NH). Anal. Calculated for C18H18BrN3O2 : C, 55.68; H, 4.67; N, 10.82. Found C, 55.48; H, 4.84; N, 10.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663337
Source datasetuspto-grants-1997_09
ORD IDord-f815ce65d13f40d9970f4b25130cb9b6
Source noteuspto-grants-1997_09