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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Diphenylmethyl)-4-[(oxiran-2-yl)methyl]piperazine | HCID 10244778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{[2-(3,4-Dimethoxyphenyl)ethyl]amino}-3-[4-(diphenylmethyl)piperazin-1-yl]propan-2-ol | HCID 3072700 | 24.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391552 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-77b79991366c412498b2fb7374b56fc8 |
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| Source note | uspto-grants-1995_02 |
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