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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087074Generated: October 27, 2026

N-(2-Aminoethyl)piperidine → (R/S)-N-[2-(1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamide

https://huagongshe.com/reaction/1087074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactantethyl (R/S)-2-(3-hydroxy-2oxo-1-pyrrolidinyl)acetateHCID 13385945—
Product(R/S)-N-[2-(1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamideHCID 131713897—

Reaction Steps

3.0 g of ethyl (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetate and 2.87 g of N-(2-aminoethyl)piperidine are heated to 100° for 4 hours under nitrogen. The excess N-(2-aminoethyl)piperidine is distilled in a high vacuum. The (R/S)-N-[2-(1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamide remaining as the residue has a melting point of 110°-111° after crystallization from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034402
Source datasetuspto-grants-1991_07
ORD IDord-9b11a3ad50784ac3b03ca220cbcaf91c
Source noteuspto-grants-1991_07