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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1632566Erstellt: 26. Oktober 2026

1-(1H-Imidazol-1-yl)ethanone → (R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetamide

https://huagongshe.com/reaction/1632566

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(1H-Imidazol-1-yl)ethanoneHCID 17174—
Eduktcis-(+-)-N-(2-(2,6-Dimethyl-1-piperidinyl)ethyl)-2-oxo-3-hydroxy-1-pyrrolidineacetamideHCID 3069833—
LösungsmittelTolueneHCID 1140—
Produkt(R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetamideHCID 53715870—

Reaktionsschritte

0.594 g of (R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamide is boiled at reflux for 4 hours with 0.222 g of N-acetylimidazole in 10 ml of toluene. The mixture is chromatographed over 21 g of aluminum oxide (activity grade III, neutral). The (R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetamide which is eluted with methylene chloride has a melting point of 120°-121° after crystallization from diethyl ether.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04476308
Quelldatensatzuspto-grants-1984_10
ORD IDord-8699c9d5ab3749c6965c6722c1bf2dd5
Quellennotizuspto-grants-1984_10