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HRID 64391생성일: 2026년 10월 24일

1-Butanol → 5alpha-Hydroxy-6beta-(3-propylamino)-cholest-7-en-3beta-ol

https://huagongshe.com/ko/reaction/64391

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanolHCID 263—
반응물TryptamineHCID 1150—
반응물tert-Butyl methyl etherHCID 15413—
반응물5,6alpha-Epoxicholest-7-en-3beta-olHCID 87226647—
생성물5alpha-Hydroxy-6beta-(3-propylamino)-cholest-7-en-3beta-olHCID 11764268359%

반응 단계

5,6α-epoxicholest-7-en-3β-ol (8.9 g, 22.1 mmol, 1 eq) and tryptamine (7.1 g, 44.1 mmol, 2 eq) were charged in a round-bottomed flask equipped with a magnetic stirrer bar. 1-Butanol (70 ml, 5 vol) was added and the mixture heated to reflux for 40 h. The reaction mixture was cooled at r.t., diluted with methyl-tertbutyl-ether (5 vol) and washed with water (5 vol) and with brine (5 vol). The organic layer was passed through a silica pad (40 g) eluted with methyl-tertbutyl-ether (3 vol) then 10% Methanol/ethyl acetate (60 vol). Fractions of interest were pooled and the solvent was removed under reduced pressure to give 5α-Hydroxy-6β-(3-propylamino)-cholest-7-en-3β-ol as a white solid (7.3 g, 59%). In same conditions, use of ethanol as solvent (40 vol) and Ca(OTf)2 as catalyst gave a 23% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447141B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-37cb1dbd7f284525ba54028279f43338
출처 메모uspto-grants-2016_09