HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 11beta-Fluoro-7alpha-{5-(methyl-nonyl-amino]pentyl}-oestra-1,3,5(10)-triene-3,17beta-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 11beta-Fluoro-3-hydroxy-7alpha-{5-[methyl-nonyl-amino]pentyl}oestra-1,3,5(10)-trien-17-one | HCID 69918018 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 11beta-Fluoro-7alpha-{5-(methyl-nonyl-amino]pentyl}-oestra-1,3,5(10)-triene-3,17beta-diol | HCID 15858645 | 38.7% |
Reaction Steps
85 mg of 11β-fluoro-3-hydroxy-7α-{5-[methyl-nonyl-amino]-pentyl}-estra-1,3,5(10)-trien-17-one is dissolved in 3 ml of methanol and mixed with 25 mg of sodium borohydride. After 30 minutes of stirring at room temperature, the solvent is drawn off in a vacuum for the most part, the residue is mixed with common salt solution, extracted 3 times with methylene chloride, dried on magnesium sulfate and concentrated by evaporation in a vacuum. Preparative thin-layer chromatography with methylene chloride/methanol=9/1+0.5% triethylamine as a mobile solvent provides 33 mg of 11β-fluoro-7α-{5-[methyl-nonyl-amino]-pentyl}-estra-1,3,5(10)-triene-3,17β-diol as a foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06780855B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-34d706f46f3a4fcda7c197d92f447698 |
| Source note | uspto-grants-2004_08 |