化工社化工社 化学情報印刷レポート · 研究参考用
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bis(2-chloroethyl)ethylamine | HCID 10848 | — |
| 反応物 | methyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochloride | HCID 18334328 | — |
| 溶媒 | Diisopropylethylamine | HCID 81531 | — |
| 生成物 | methyl (S)-3-tert-butoxycarbonylamino-2-(4-ethylpiperazin-1-yl)propanoate | HCID 86667916 | 40.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US09365529B2 |
|---|
| 出典データセット | uspto-grants-2016_06 |
|---|
| ORD ID | ord-86369a9a7d504d26bfd8f004bbe78a9a |
|---|
| 出典メモ | uspto-grants-2016_06 |
|---|