Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55148Generated: October 25, 2026

1,1'-Carbonyldiimidazole → 2-Methyl-N-[4-(pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]benzamide

https://huagongshe.com/reaction/55148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
Reactant4,5-Dihydropyrrolo[1,2-a]quinoxalineHCID 11805181—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-N-[4-(pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]benzamideHCID 1534066834.4%

Reaction Steps

A mixture of 0.51 g of 4-[(2-methylbenzoyl)amino]benzoyl chloride and 0.36 g of 1,1'-carbonyldiimidazole in 6 ml of tetrahydrofuran is stirred at room temperature for 1 hour. To the reaction mixture is added 0.17 g of 4,5-dihydropyrrolo-[1,2-a]-quinoxaline followed by heating at reflux for 60 hours. The volatiles are concentrated vacuo to a residue which is dissolved in ethyl acetate. The organic layer is washed with 1N HCl, 1M NaHCO3, brine, dried with Na2SO4 and filtered through hydrous magnesium silicate. The volatiles are concentrated in vacuo to a residue which is chromatographed by elution with 1:2 ethyl acetate-hexanes to give 0.14 g of the desired product as a white solid, m.p. 206°-207° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624923
Source datasetuspto-grants-1997_04
ORD IDord-662f6321882140b28a27444553afc4a9
Source noteuspto-grants-1997_04