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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

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N6-Boc-N2-Cbz-DL-lysineHCID 294900—
반응물Sodium borohydrideHCID 4311764—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(5-Benzyloxycarbonylamino-6-hydroxy-hexyl)-carbamic acid tert-butyl esterHCID 1449853391%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729258B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-63f6af641c264c22a1969b41cd190fcd
출처 메모uspto-grants-2014_05