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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274908Generated: October 30, 2026

Benzylamine → 1-(Benzylamino)-3-{4-[4,4-bis(4-fluorophenyl)butyl]piperazin-1-yl}propan-2-ol

https://huagongshe.com/reaction/274908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantPotassium CarbonateHCID 11430—
Reactant1-[4,4-Bis(4-fluorophenyl)butyl]-4-[(oxiran-2-yl)methyl]piperazineHCID 20088935—
SolventDimethylformamideHCID 6228—
Product1-(Benzylamino)-3-{4-[4,4-bis(4-fluorophenyl)butyl]piperazin-1-yl}propan-2-olHCID 307270210.1%

Reaction Steps

3.86 g (0.01 mol) of 1-[4,4-bis(4-fluorophenyl)butyl]-4-(2,3-epoxypropyl)piperazine and 1 g (0.01 mol) of benzylamine were refluxed with heating together with 200 ml of DMF for 24 hours in the presence of a catalytic amount of an alkali such as potassium carbonate. DMF was distilled off under reduced pressure, and a residue was extracted with ethyl acetate. After washing with water and drying, the ethyl acetate was distilled off under reduced pressure to obtain 5 g of a crude subject compound of a viscous liquid. The obtained compound was refined by flush chromatography and fractional thin-layer chromatography with solvent mixtures of ethyl acetate--methanol and methylene chloride--methanol respectively to obtain 0.5 g of the subject compound in a viscous liquid state.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391552
Source datasetuspto-grants-1995_02
ORD IDord-66ceb95e964e434cb496564707c9ef55
Source noteuspto-grants-1995_02