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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 874581Erstellt: 24. Oktober 2026

Bis(2-chloroethyl)ethylamine → methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate

https://huagongshe.com/de/reaction/874581

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(2-chloroethyl)ethylamineHCID 10848—
Eduktmethyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochlorideHCID 18334328—
LösungsmittelDiisopropylethylamineHCID 81531—
Produktmethyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoateHCID 8666791640,4%

Reaktionsschritte

A solution of 5.0 g (19.6 mmol) of commercial methyl (S)-2-amino-3-tert-butoxycarbonylaminopropanoate hydrochloride and 3.3 g (19.6 mmol) of bis(2-chloroethyl)ethylamine in 50 ml of N,N-diisopropylethylamine is heated at 127° C. for 5 h. After evaporation of a maximum amount of diisopropylethylamine, the reaction medium is diluted with ethyl acetate and washed with an aqueous solution of sodium hydroxide having a concentration of 1N. The organic phase obtained is then washed with water, dried over magnesium sulfate, filtered and concentrated under vacuum. The crude product obtained is purified by chromatography on silica gel, elution being carried out with a 30/70 heptane/ethyl acetate mixture. 2.5 g (40%) of methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate are obtained in the form of an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08980897B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-38cfb5e90a2341bab8cb438e7d52f29b
Quellennotizuspto-grants-2015_03