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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901691Generated: October 25, 2026

Dimethylformamide → [3-(4-{1-[4-(4-Chloro-phenoxy)-phenyl]-2-phenethyl-1h-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amine

https://huagongshe.com/reaction/901691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(4-Chlorophenoxy)anilineHCID 7578—
Reactant2-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanoneHCID 86591969—
SolventWaterHCID 962—
Product[3-(4-{1-[4-(4-Chloro-phenoxy)-phenyl]-2-phenethyl-1h-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amineHCID 59698958—

Reaction Steps

To a stirred solution of 4-amino-4′-chlorodiphenyl ether (1.2 eq., 6.2 mmol) in anhydrous DMF (10 mL) DIEA (3 eq. 16 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (5.2 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 extracted 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 ˜22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361678B2
Source datasetuspto-grants-2008_04
ORD IDord-9224dfcf93cc4375b1e84b0d23d25eaf
Source noteuspto-grants-2008_04