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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1657258생성일: 2026년 10월 25일

N-[(S)-alpha-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidine → HCID 178455618, 화합물

https://huagongshe.com/reaction/1657258

반응식

참여 물질

역할이름HCID투입량
반응물N-[(S)-alpha-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidineHCID 22845096—
반응물(1RS,2R,3S)-3-amino-4-cyclohexyl-1-(2-furyl)-1,2-butanediolHCID 57084513—
생성물HCID 178455618HCID 178455618—

반응 단계

In an analogous manner to that described in Example 13, by reacting (1RS,2R,3S)-3-amino-4-cyclohexyl-1-(2-furyl)-1,2-butanediol with N-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidine there was obtained (S)-α-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamamido]-N-[(1S,2R,3RS)-1-(cyclohexylmethyl)-2,3-dihydroxy-3-(2-furyl)propyl]imidazole-4-propionamide (1:1 mixture of epimers) as a pale yellow solid, MS: 657 (M+H)+. The more polar epimer, (S)-α-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamamido]-N-[(1S,2R,3R or S)-1-(cyclohexylmethyl)-2,3-dihydroxy-3-(2-furyl)propyl]imidazole-4-propionamide, MS: 657 (M+H)+, can be separated from the above mixture by chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05256645
출처 데이터셋uspto-grants-1993_10
ORD IDord-03107b272b024ac1800b138c14d821e1
출처 메모uspto-grants-1993_10