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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282124Generated: October 31, 2026

Potassium Iodide → N-(4-(1-(4-(4-fluorophenyl)piperazin-1-yl)-1-methylethyl)phenylmethyl)acetamide dihydrochloride monohydrate

https://huagongshe.com/reaction/1282124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantAniline, N,N-bis(2-chloroethyl)-p-fluoro-HCID 30941—
ReactantN-(4-(1-amino-1-methylethyl)phenylmethyl)acetamideHCID 18423109—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-(4-(1-(4-(4-fluorophenyl)piperazin-1-yl)-1-methylethyl)phenylmethyl)acetamide dihydrochloride monohydrateHCID 1842314522.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N-(4-(1-amino-1-methylethyl)phenylmethyl)-acetamide (1.55 g) and N,N-di(2-chloroethyl)-4-fluoroaniline (1.5 g) in dimethyl sulfoxide (30 ml) were added potassium carbonate (3.12 g) and potassium iodide (2.50 g) and the mixture was stirred at 80° C. for 24 hr. The reaction mixture was poured into water (300 ml) and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated and the obtained residue was purified by silica gel chromatography (developing solvent; ethyl acetate:hexane=3:1) and treated with 1M hydrochloric acid-ether in ethanol to give the title compound (0.33 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455528B1
Source datasetuspto-grants-2002_09
ORD IDord-e5489caa0e9b47868fbcc60aa2f95bca
Source noteuspto-grants-2002_09