Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227454Generated: November 1, 2026

Methane → 4-Ethyl-4-phenyl-2-(2-phenylquinolin-4-yl)-imidazoline

https://huagongshe.com/reaction/2227454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant2-Phenylbutane-1,2-diamineHCID 21149—
ReactantMethyl 2-phenyl-4-quinolinecarboxylateHCID 609693—
ReactantTrimethylaluminumHCID 16682925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product4-Ethyl-4-phenyl-2-(2-phenylquinolin-4-yl)-imidazolineHCID 178435244—

Reaction Steps

2-Phenylbutane-1,2-diamine (328 mg, 2.0 mmol) in 4.4 mL of toluene is added dropwise to a stirred solution of trimethylaluminum (2.0 M, 1 mL) in 5 mL of toluene at below 10° C. under nitrogen. At the end of methane evolution, methyl-2-phenyl-4-quinolinecarboxylate (263 mg, 1 mmol) in 2 mL of toluene is gradually added at room temperature. The reaction mixture is refluxed for 3 hours under nitrogen. After cooling, the solution is treated with 1 mL of water, diluted with 1 mL of methanol and 1 mL of methylene chloride, and refluxed for 15 minutes. After separation of organic solvent and solvent evaporation, the residue is purified over silica gel chromatography eluting with 5-10% MeOH/CH2Cl2. The corresponding compound is obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413982B1
Source datasetuspto-grants-2002_07
ORD IDord-3653a529e44440ccb38978cef2f77d49
Source noteuspto-grants-2002_07