戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1966121作成日:2026年10月26日

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

https://huagongshe.com/reaction/1966121

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-chloroethyl)ethylamineHCID 10848—
反応物methyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochlorideHCID 18334328—
溶媒DiisopropylethylamineHCID 81531—
生成物methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoateHCID 8666791640.4%

反応手順

A solution of 5.0 g (19.6 mmol) of commercial methyl (S)-2-amino-3-tert-butoxycarbonylamino-propanoate 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08420632B2
出典データセットuspto-grants-2013_04
ORD IDord-199a04bd1f6541679df7a3cf7b8fa495
出典メモuspto-grants-2013_04