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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274906Generated: October 30, 2026

Homoveratrylamine → 1-{[2-(3,4-Dimethoxyphenyl)ethyl]amino}-3-[4-(diphenylmethyl)piperazin-1-yl]propan-2-ol

https://huagongshe.com/reaction/274906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoveratrylamineHCID 8421—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Diphenylmethyl)-4-[(oxiran-2-yl)methyl]piperazineHCID 10244778—
SolventDimethylformamideHCID 6228—
Product1-{[2-(3,4-Dimethoxyphenyl)ethyl]amino}-3-[4-(diphenylmethyl)piperazin-1-yl]propan-2-olHCID 307270024.5%

Reaction Steps

3.08 g (0.01 mol) of 1-(diphenylmethyl)-4-(2,3-epoxypropyl)piperazine and 2 g (0.01 mol) of 2-(3,4-dimethoxyphenyl)ethylamine 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, and after washing with water and drying, the ethyl acetate was distilled off under reduced pressure to obtain 5.1 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 1.2 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-77b79991366c412498b2fb7374b56fc8
Source noteuspto-grants-1995_02