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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48957생성일: 2026년 10월 23일

Dehydroepiandrosterone → Dehydroepiandrosterone

https://huagongshe.com/ko/reaction/48957

반응식

참여 물질

역할이름HCID투입량
반응물DehydroepiandrosteroneHCID 5881—
반응물22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONEHCID 69625815—
생성물DehydroepiandrosteroneHCID 5881—
생성물HCID 178420941HCID 178420941—

반응 단계

The synthesis of 22,29-epoxy-3,29-dihydroxy-14β-stigmastan-15-one (260) can be accomplished in ten steps from dehydroisoandrosterone (247). Catalytic hydrogenation of the Δ5 carbon-carbon double bond in compound 247 yields compound 250, which contains a trans-fused A/B ring-system. Compound 247 is dissolved in EtOAc and 10% Pd/C is added. The mixture is stirred under H2 at room temperature overnight. Filtration through celite and concentration yields compound 250, which can be used directly in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706701B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-d863766c08014899a9c4dffcca1796e9
출처 메모uspto-grants-2004_03