HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Osaterone acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 14306878 | HCID 14306878 | — |
| Solvent | Water | HCID 962 | — |
| Product | Osaterone acetate | HCID 114992 | 72.1% |
Reaction Steps
A mixture of 2.35 g of 17α-acetoxy-6β-chloro-7α-mesyloxy-2-oxa-4-pregnene-3,20-dione, 0.83 g of potassium acetate and 0.88 ml of dimethyl sulfoxide was stirred at room temperature for 12 hours. Ice-cooled water was poured into the reaction mixture, and the precipitated crystals were collected by filtration to give 1.37 g of 17α-acetoxy-6-chloro-2-oxapregna-4,6-diene-3,20-dione. The 1H NMR spectrum of this compound was the same as that of the compound produced in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04914106 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-745a2b3923b4401790426acdbf2986f1 |
| Source note | uspto-grants-1990_04 |