Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026528생성일: 2026년 10월 25일
1,1'-Carbonyldiimidazole → (5-Benzyloxycarbonylamino-6-hydroxy-hexyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1026528
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | N6-Boc-N2-Cbz-DL-lysine | HCID 294900 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-Benzyloxycarbonylamino-6-hydroxy-hexyl)-carbamic acid tert-butyl ester | HCID 14498533 | 91% |
반응 단계
To a stirred solution of 2-benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexanoic acid (Cbz-Lys(Boc)-OH) (Chem-Impex International, 3.8 g, 10 mmol) in THF (25 mL) in a 100 mL round flask was added 1,1′-carbonyldiimidazole (CDI) (1.7 g, 10.5 mmol) at room temperature. After 20 minutes, the THF solution was transferred via a Teflon canula (φ=2 mm) to a stirred solution of sodium borohydride (0.75 g, 20 mmol) in water (10 mL) in a 1 L round flask immersed in a water bath at 5-10° C. The addition caused a strong evolution of hydrogen gas and the mixture was stirred for a couple of hours. The volatiles were then removed on a rotovap, and the residue was dissolved in ethyl acetate (150 mL). The ethyl acetate solution was extracted successively with cold 1 N HCl (2×50 mL), saturated sodium bicarbonate solution (2×50 mL), brine (100 mL), and was dried with anhydrous sodium sulfate. The dried ethyl acetate solution was then pass through a one inch flash pad of silica gel, and concentrated to provide a colorless solid (3.3 g, 91%), TLC Rf=0.24 (95:5:2 EtOAc:MeOH:H2O).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08729258B2 |
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| 출처 데이터셋 | uspto-grants-2014_05 |
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| ORD ID | ord-63f6af641c264c22a1969b41cd190fcd |
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| 출처 메모 | uspto-grants-2014_05 |
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