Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031811생성일: 2026년 10월 25일
Triethylamine → N-(Nalpha-benzyloxycarbonyl-Nepsilon-tert-butoxycarbonyl-L-lysyl)-L-proline tert-butyl ester
https://huagongshe.com/reaction/1031811
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Diethyl cyanophosphonate | HCID 76257 | — |
| 반응물 | IN2-(benzyloxycarbonyl)-N6-(tert-butoxycarbonyl)-L-lysine | HCID 98765 | — |
| 반응물 | L-Proline 1,1-dimethylethyl ester | HCID 6453108 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(Nalpha-benzyloxycarbonyl-Nepsilon-tert-butoxycarbonyl-L-lysyl)-L-proline tert-butyl ester | HCID 14010667 | 73.5% |
반응 단계
In 30 ml of N,N-dimethylformamide are dissolved 2.4 g of L-proline tert-butyl ester and 5.87 g of Nα -benzyloxycarbonyl-Nε -tert-butoxycarbonyl-L-lysine, and 3 g of diethyl phosphorocyanidate is added dropwise to the solution under ice-cooling. After stirring for 30 minutes, a solution of 1.42 g of triethylamine in 5 ml of N,N-dimethylformamide is added to the mixture, followed by stirring under ice-cooling for 1 hour and then at room temperature for 2 hours. 500 ml of water is added to the reaction mixture, and the mixture is extracted with 300 ml of ethyl acetate. The extract is washed with aqueous dilute phosphoric acid, 0.1N aqueous sodium hydroxide and water, successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting oily material is purified by silica gel column chromatography (hexane:ethyl acetate=2:1 to 1:1) to give 5.5 g of N-(Nα -benzyloxycarbonyl-Nε -tert-butoxycarbonyl-L-lysyl)-L-proline tert-butyl ester as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04954625 |
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| 출처 데이터셋 | uspto-grants-1990_09 |
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| ORD ID | ord-c9f50474bb534b5284b2b42befb7309b |
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| 출처 메모 | uspto-grants-1990_09 |
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