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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501761생성일: 2026년 10월 26일

5-Hexenoic Acid → N-((2S,3R)-4-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-1-(3,5-dichlorophenyl)-3-hydroxy-butan-2-yl)hex-5-enamide

https://huagongshe.com/reaction/501761

반응식

참여 물질

역할이름HCID투입량
반응물5-Hexenoic AcidHCID 15308—
반응물(2R,3S)-1-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-3-amino-4-(3,5-dichloro-phenyl)butan-2-olHCID 59423767—
생성물N-((2S,3R)-4-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-1-(3,5-dichlorophenyl)-3-hydroxy-butan-2-yl)hex-5-enamideHCID 6846504191.3%

반응 단계

Step DQ (1): 5-Hexenoic acid (Alfa Aesar, 0.096 mmole) and (2R,3S)-1-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-3-amino-4-(3,5-dichloro-phenyl)butan-2-ol (0.04 mmol, from Preparation BG) were coupled by a procedure analogous to Step DL (1) to afford 20 mg of N-((2S,3R)-4-((1S,3R)-3-(allyloxy)-6-methoxy-2,3-dihydro-1H-inden-1-ylamino)-1-(3,5-dichlorophenyl)-3-hydroxy-butan-2-yl)hex-5-enamide as a clear oil. LC-MS Rt 2.1 min (method A), (M+H)+=547.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772221B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-9e894e0763a744c49e557b90f2060541
출처 메모uspto-grants-2010_08