Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433048생성일: 2026년 10월 26일
Diisopropylethylamine → 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester
https://huagongshe.com/reaction/1433048
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzyl 1-methyl-2-oxoethylcarbamate | HCID 563116 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | methyl (2S)-2-aminopentanoate hydrochloride | HCID 14118488 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester | HCID 69027995 | 38.6% |
반응 단계
To a solution of [1-methyl-2-oxo-ethyl]-carbamic acid benzyl ester (12.3 g, 69 mmol) and norvaline methylester hydrochloride (11.6 g, 69 mmol) in MeOH (300 mL) is added diisopropyl ethyl amine (9.4 g, 73 mmol) and 2 drops of acetic acid. After 10 min., ZnCl2 (9.46 g, 69 mmol) and sodium cyanoborohydride (8.72 g, 14 mmol) is added. The solution is stirred at ambient for 16 h. The solution is then concentrated. The residue is dissolved in EtOAc and 1N KHSO4. The organic layer is washed with 1N KHSO4, H2O, and sat. NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatograghy eluting with a gradient of 20% EtOAc/hexane to 40% EtOAc/hexanes. The title compound (8.6 gm, 26.6 mmol) is obtained as a foam. MS (ion spray) m/z 323, (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07612075B2 |
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| 출처 데이터셋 | uspto-grants-2009_11 |
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| ORD ID | ord-aa4a4c2600c048e99a1e0176bd434d07 |
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| 출처 메모 | uspto-grants-2009_11 |
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