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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275617생성일: 2026년 10월 26일

2-{[(Tert-butoxy)carbonyl]amino}-3-(pyridin-4-yl)propanoic acid → alpha-amino-N-[(1S,2R,3 S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(pyridin-4-yl)propionamide

https://huagongshe.com/reaction/275617

반응식

참여 물질

역할이름HCID투입량
반응물2-{[(Tert-butoxy)carbonyl]amino}-3-(pyridin-4-yl)propanoic acidHCID 3294373—
반응물(1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediolHCID 14930738—
생성물alpha-amino-N-[(1S,2R,3 S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(pyridin-4-yl)propionamideHCID 67813325—

반응 단계

In an analogous manner to that described above, by the condensation of N-(tert-butoxycarbonyl)-3-(pyridin-4-yl)-D,L-alanine [J. Gen. Chem. USSR, 40, 2488 (1970)]and (1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediol followed by acidic hydrolysis there were obtained (S or R)-α-amino-N-[(1S,2R,3 S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(pyridin-4-yl)propionamide, MS: 267 (M+H)+, and (R or S)-α-amino-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-3-(pyridin-4-yl)propionamide, MS: 267 (M+H)+, each as a colourless foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393875
출처 데이터셋uspto-grants-1995_02
ORD IDord-89370d97ea7d4caeafb1954734c73cae
출처 메모uspto-grants-1995_02