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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582465Generated: November 1, 2026

Triethylamine → 4-(4-chloro-phenyl)-2-(4-methoxy-phenyl)-5-(4-nitro-phenyl)-4,5-dihydro-1H-imidazole

https://huagongshe.com/reaction/1582465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 4-methoxybenzimidate hydrochlorideHCID 12270046—
Reactant1-(4-Chloro-phenyl)-2-(4-nitro-phenyl)-ethane-1,2-diamineHCID 22721067—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product4-(4-chloro-phenyl)-2-(4-methoxy-phenyl)-5-(4-nitro-phenyl)-4,5-dihydro-1H-imidazoleHCID 13553085337%

Reaction Steps

To a solution of 1-(4-chloro-phenyl)-2-(4-nitro-phenyl)-ethane-1,2-diamine (200 mg, 0.685 mmol) and ethyl 4-methoxy-benzimidate hydrochloride (148 mg, 0.686 mmol) in ethanol (5 mL) was added triethylamine (0.11 mL, 0.79 mmol). The reaction mixture was heated at reflux for 12 h. The solvent was removed to give a clear oil. It was then taken in methylene chloride (2 mL) and aqueous sodium carbonate. The product was extracted with methylene chloride (2×20 mL). The organic layers were washed with brine (1×5 mL), dried (Na2SO4) and concentrated. Purification of the crude residue by Biotage flash chromatography eluting with 70% ethyl acetate in hexanes gave 4-(4-chloro-phenyl)-2-(4-methoxy-phenyl)-5-(4-nitro-phenyl)-4,5-dihydro-1H-imidazole (103 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734302B2
Source datasetuspto-grants-2004_05
ORD IDord-711ad68918dd4b8eb12008c1ca8a3bfa
Source noteuspto-grants-2004_05