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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237052Generated: October 26, 2026

Dimethylformamide → [3-(4-{1-[4-(biphenyl-4-yloxy)-phenyl]-2-butyl-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amine

https://huagongshe.com/reaction/2237052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(4-Phenylphenoxy)anilineHCID 247124—
Reactant2-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanoneHCID 86591969—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product[3-(4-{1-[4-(biphenyl-4-yloxy)-phenyl]-2-butyl-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amineHCID 5969891613%

Reaction Steps

To a stirred solution of 4-(biphenyl-4-oxy)aniline (1.2 eq., 2.5 mmol) in anhydrous DMF (5 mL) DIEA (3 eq. 6 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (2.4 mmol), according to General Procedure R2. The reaction mixture was stirred under nitrogen at rt until completion, as indicated by TLC or HPLC. The reaction mixture was then diluted with cold H2O and the product was isolated in EtOAc. The combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of solvent in vacuuo afforded the desired product. The crude alkylated aniline was purified by chromatography (Silica gel). Pure product obtained from 2-4% MeOH/DCM (yield ˜13%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714013B2
Source datasetuspto-grants-2010_05
ORD IDord-381a7f6b042342cd99d9f961a5dcf490
Source noteuspto-grants-2010_05