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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327344생성일: 2026년 10월 26일

Acetic Acid → Boc-His(Ts) 1(S)-cyclohexylmethyl-2(S)-hydroxy-4-oxo-4-cyclohexyl-butylamide

https://huagongshe.com/reaction/327344

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물TolueneHCID 1140—
반응물Cyclohexyl methyl ketoneHCID 13207—
반응물Ammonium ChlorideHCID 25517—
반응물18-Crown-6HCID 28557—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물Boc-His(Ts) 3-cyclohexylalaninalHCID 131717823—
용매TetrahydrofuranHCID 8028—
생성물Boc-His(Ts) 1(S)-cyclohexylmethyl-2(S)-hydroxy-4-oxo-4-cyclohexyl-butylamideHCID 13171782415%

반응 단계

To a 0.5N potassium bis-trimethylsilylamide solution in toluene (9.2 ml, 4.60 mmol, 2.5 eq) is added dropwise at -78° C. cyclohexyl methyl ketone (0.58 g, 4.60 mmol, 2.5 eq) in THF (9 ml) with stirring under a nitrogen atmosphere over 10 minutes. After 20 minutes stirring at the same temperature, 18-crown-6 (1.216 g, 4.60 mmol, 2.5 eq) in THF (10 ml) is dropwise added to the mixture over two minutes. Further, the dipeptidealdehyde [14a] (1.0 g, 1.83 mmol) in THF (10 ml) is dropwise added over 15 minutes at -78° C., and the mixture is stirred for one hour at the same temperature. The reaction is quenched by adding a solution of acetic acid (0.60 g, 10 mmol, 5.5 eq) in THF (10 ml) and after the addition of saturated aqueous ammonium chloride (30 ml) the mixture is extracted with ethyl acetate (50 ml×3). The organic layer is washed with saturated aqueous sodium chloride, dried over MgSO4, concentrated to dryness in vacuo, and purified with silica gel chromatography (Lobar column, CH2Cl2 :MeOH=95:5) to obtain Boc-His(Ts)-1(S)-cyclohexylmethyl-2(S)-hydroxy-4-oxo-4-cyclohexyl-butylamide [10b] (0.18 g, 15%) in amorphous powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05272268
출처 데이터셋uspto-grants-1993_12
ORD IDord-23183dfc9f25499d96b37d8d228aa3f8
출처 메모uspto-grants-1993_12