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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275621생성일: 2026년 10월 24일

(1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediol → rac-alpha-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(furan-2-yl)propionamide

https://huagongshe.com/ko/reaction/275621

반응식

참여 물질

역할이름HCID투입량
반응물(1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediolHCID 14930738—
반응물Cbz-3-(2-furyl)-DL-alanineHCID 20088483—
생성물rac-alpha-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(furan-2-yl)propionamideHCID 57246147—

반응 단계

In an analogous manner to that described above, by the condensation of (RS)-α-(1-benzyloxyformamido)-3-(furan-2-yl)propionic acid [J. Biol. Chem. 171, 383 (1947)]and (1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediol followed by catalytic hydrogenation there was obtained rac-α-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(furan-2-yl)propionamide, MS: 365 (M+H)+, as a colourless foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393875
출처 데이터셋uspto-grants-1995_02
ORD IDord-94f259c8e7ee40429f6cefed67bda66f
출처 메모uspto-grants-1995_02