Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49272Generated: October 30, 2026

Dimethylformamide → 1-[6-(4-Bromophenoxy)hexyl]-4-phenyl-3-(4-pyridyl)-2-imidazolidinone

https://huagongshe.com/reaction/49272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-4-((6-bromohexyl)oxy)benzeneHCID 22494750—
Reactant[5-phenyl-1-(4-pyridyl)tetrahydro-1H-2-imidazolyliden]aminomethane-nitrileHCID 178512069—
Product1-[6-(4-Bromophenoxy)hexyl]-4-phenyl-3-(4-pyridyl)-2-imidazolidinoneHCID 10311228—

Reaction Steps

To a solution of [5-phenyl-1-(4-pyridyl)tetrahydro-1H-2-imidazolyliden] aminomethane-nitrile (0.1 g, 0.38 mmol) in 6 mL of DMF at 0° C. was added sodium hydride (75% dispersion in mineral oil, 24 mg) in one portion. The mixture was stirred at room temperature for 20 min and then 1-[(6-bromohexyl)oxy]-4-bromobenzene (192 mg, 0.57 mmol) dissolved in DMF (4 mL) was added dropwise. The resulting mixture was stirred and heated at 80° C. for 16 hours. The reaction was quenched with water and aqueous solution was extracted with ether (3×20 mL). The organic layers were combined, washed with NaCl(sat.), dried over MgSO4, and concentrated under reduced pressure to give the crude residue, which was subjected to purification by chromatography elution with ethyl acetate and methanol (20:1) to afford the product (i.e., Compound 15) as a white solid (90 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706739B2
Source datasetuspto-grants-2004_03
ORD IDord-6ea8d5dd868d4ea28cb4edcfc909677c
Source noteuspto-grants-2004_03