HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20206891, compound → HCID 70447180, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20206891 | HCID 20206891 | — |
| Reactant | HCID 86741440 | HCID 86741440 | — |
| Product | HCID 70447180 | HCID 70447180 | — |
Reaction Steps
The process described in the last paragraph of Example 6 was repeated except that (8-hexanamidooctyl)triphenylphosphonium bromide was used in place of (9-carboxynonyl)triphenylphosphonium bromide. The hydrogenation process described in the second paragraph of Example 6 was then repeated using the N-[9-(3-benzyloxy-17β-hydroxyoestra-1,3,5(10)-trien-7α-yl)non-8-enyl]hexanamide thus obtained as starting material, and there was thus obtained as an oil N-[9-(3,17β-dihydroxyoestra-1,3,5(10)-trien-7α-yl)nonyl]hexanamide, the structure of which was confirmed by proton magnetic resonance and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659516 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-5da3f0d14253409ba5ab6b10b780aafd |
| Source note | uspto-grants-1987_04 |