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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48957Erstellt: 23. Oktober 2026

Dehydroepiandrosterone → Dehydroepiandrosterone

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDehydroepiandrosteroneHCID 5881—
Edukt22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONEHCID 69625815—
ProduktDehydroepiandrosteroneHCID 5881—
ProduktHCID 178420941HCID 178420941—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706701B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-d863766c08014899a9c4dffcca1796e9
Quellennotizuspto-grants-2004_03