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HRID 2202193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/2202193

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-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365529B2
出典データセットuspto-grants-2016_06
ORD IDord-86369a9a7d504d26bfd8f004bbe78a9a
出典メモuspto-grants-2016_06