Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → HCID 15927688, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyl L-alanyl-L-prolinate | HCID 12939800 | — |
| 반응물 | Ethyl 2-bromo-9-phthalimidononanoate | HCID 13622534 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | HCID 15927688 | HCID 15927688 | 13.1% |
반응 단계
A solution of ethyl 2-bromo-9-phthalimidononanoate [prepared according to Chem. Pharm. Bull. 34, 2078 (1986)] (3 g), L-alanyl-L-proline tertiary butylester (1 g) and triethylamine (0.8 ml) in acetonitrile (200 ml) is subjected to 60 hours' reflux. Acetonitrile is distilled off under reduced pressure, and the residue is dissolved in ethyl acetate. The solution is dehydrated with anhydrous sodium sulfate, and thereafter is concentrated to obtain an oily residue. When this substance is applied to a silica gel chromatography (ethyl acetate:n-hexane=3:1) for separative purification, 310 mg of N-[1(R)-ethoxycarbonyl-8-phthalimidooctyl]-L-alanyl-L-proline tertiary butylester is obtained as a colorless oil from the first effluence.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04897483 |
| 출처 데이터셋 | uspto-grants-1990_01 |
| ORD ID | ord-634fc89166d84c45b81d6c9f9789ba58 |
| 출처 메모 | uspto-grants-1990_01 |