HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dehydroepiandrosterone → Dehydroepiandrosterone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dehydroepiandrosterone | HCID 5881 | — |
| Reactant | 22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONE | HCID 69625815 | — |
| Product | Dehydroepiandrosterone | HCID 5881 | — |
| Product | HCID 178420941 | HCID 178420941 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06949533B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-0cda258f352b4f39b8edc6215f598f38 |
| Source note | uspto-grants-2005_09 |