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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855986Generated: November 1, 2026

1,2-Ethanediamine, N1-phenyl- → 1-[2-Hydroxy-3-(2-methoxyphenyloxy)-propyl]-4-(2-anilino-ethylamino)-piperidine

https://huagongshe.com/reaction/1855986

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1-phenyl-HCID 74270—
Reactant1-[2-Hydroxy-(2-methoxyphenyloxy)-propyl]-piperidin-4-oneHCID 23347344—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product1-[2-Hydroxy-3-(2-methoxyphenyloxy)-propyl]-4-(2-anilino-ethylamino)-piperidineHCID 23347339—

Reaction Steps

A solution of 16.7 g of 1-[2-hydroxy-3-(2-methoxyphenyloxy)-propyl]-piperidine-4-one and 10.5 g of N-(2-aminoethyl)-aniline in 250 ml of methanol, with the addition of 1 g of a 5% platinum on charcoal catalyst is hydrogenated at room temperature and under normal pressure until 1 molar equivalent of hydrogen has been taken up. The catalyst is thereafter removed by filtration and the filtrate is concentrated under reduced pressure. The residue is freed from excess starting material in a bulb tube at 0.3 mm Hg and 120° C. oven temperature to yield as distillation residue 1-[2-hydroxy-3-(2-methoxyphenyloxy)-propyl]-4-(2-anilino-ethylamino)-piperidine, which can be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217350
Source datasetuspto-grants-1980_08
ORD IDord-1fcbedd729314820aa69c3583c3bac4b
Source noteuspto-grants-1980_08