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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2202193생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2202193

반응식

참여 물질

역할이름HCID투입량
반응물Bis(2-chloroethyl)ethylamineHCID 10848—
반응물methyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochlorideHCID 18334328—
용매DiisopropylethylamineHCID 81531—
생성물methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoateHCID 8666791640.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365529B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-86369a9a7d504d26bfd8f004bbe78a9a
출처 메모uspto-grants-2016_06