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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289236Generated: October 30, 2026

Benzoyl Peroxide → HCID 135838176, compound

https://huagongshe.com/reaction/2289236

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]quina- zolin-3-yl)pivalamide as an off-white solid. (1.4 g, 57%) 1H NMRi (DMSO-d61 200MHz) δ: 1.27(s, 9H, t-butyl); 5.26(s, 2H, CH2Br'i; 7.63-7.81(m, 3H, Ar); 8.26(dd, J=7.6, 2.0 Hz, 1H, Ar); 9.81(dd, J =7.8, 2.0 Hz, 1H, Ar); 11.27(s, 1H, NH); 12.33(s, 1H, NH). Anal Calculated for C18H18BrN3 02 : 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 numberUS06090941
Source datasetuspto-grants-2000_07
ORD IDord-2c6d852fd2f84ce59579aedfe37435c8
Source noteuspto-grants-2000_07