HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dehydroepiandrosterone → Dehydroepiandrosterone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dehydroepiandrosterone | HCID 5881 | — |
| Edukt | 22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONE | HCID 69625815 | — |
| Produkt | Dehydroepiandrosterone | HCID 5881 | — |
| Produkt | HCID 178420941 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06706701B1 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-d863766c08014899a9c4dffcca1796e9 |
| Quellennotiz | uspto-grants-2004_03 |