Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 874581생성일: 2026년 10월 25일
Bis(2-chloroethyl)ethylamine → methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate
https://huagongshe.com/reaction/874581
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Bis(2-chloroethyl)ethylamine | HCID 10848 | — |
| 반응물 | methyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochloride | HCID 18334328 | — |
| 용매 | Diisopropylethylamine | HCID 81531 | — |
| 생성물 | methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate | HCID 86667916 | 40.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08980897B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-38cfb5e90a2341bab8cb438e7d52f29b |
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| 출처 메모 | uspto-grants-2015_03 |
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