Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407919생성일: 2026년 10월 25일
tert-Butyl 4-oxopiperidine-1-carboxylate → (S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acid
https://huagongshe.com/reaction/407919
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | N-alpha-Benzyloxycarbonyl-L-ornithine | HCID 7010490 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acid | HCID 58787298 | — |
반응 단계
(S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (50 g, 188 mmol) was dissolved in THF (800 mL) and water (100 mL). Tert-butyl 4-oxopiperidine-1-carboxylate (37 g, 188 mmol) was added and the reaction was stirred for 1 hour. The reaction was cooled to 0° C. and sodium cyanoborohydride (12 g, 188 mmol) was added and the reaction stirred at ambient temperature overnight. The reaction was concentrated to provide (S)-2-(benzyloxycarbonylamino)-5-(1-(tert-butoxycarbonyl)piperidin-4-ylamino)pentanoic acid, which was used directly in the next step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08754226B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-3d3b236612484374bc9cb5e60d718c74 |
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| 출처 메모 | uspto-grants-2014_06 |
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