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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54087생성일: 2026년 10월 24일

(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutane → 2-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide

https://huagongshe.com/ko/reaction/54087

반응식

참여 물질

역할이름HCID투입량
반응물(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutaneHCID 9861019—
반응물Tert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 86746253—
용매MethanolHCID 887—
생성물2-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamideHCID 56998348—

반응 단계

A solution of 0.60 g of tert.butyl 1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide and 0.66 g of 3(S)-(benzyloxyformamido)-1,2(S)-epoxy-4-phenylbutane in 20 ml of methanol was heated at reflux under argon for 16 hours and then evaporated to give a clear oil. The two diastereomeric products were separated by flash chromatography on silica gel using n-hexane/ethyl acetate (3:1) for the elution. There were obtained 268 mg of isomer A of 2-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-N-tert.butyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-1-carboxamide, MS: m/e 569 [M+H]+, and 65 mg of isomer B of the same compound; MS: m/e 569 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620987
출처 데이터셋uspto-grants-1997_04
ORD IDord-97dce27546ba4ce5a356cafcb5e7c7d7
출처 메모uspto-grants-1997_04