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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202193Generated: October 25, 2026

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

https://huagongshe.com/reaction/2202193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-chloroethyl)ethylamineHCID 10848—
Reactantmethyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochlorideHCID 18334328—
SolventDiisopropylethylamineHCID 81531—
Productmethyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoateHCID 8666791640.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-86369a9a7d504d26bfd8f004bbe78a9a
Source noteuspto-grants-2016_06