HuagongsheHuagongshe Chemistry Print Report · For research reference only
16alpha-Hydroxyprednisolone → 11beta,17,21-Trihydroxy-16alpha-(2-phenyl-2-propenyloxy)-pregna-1,4-diene-3,20-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 16alpha-Hydroxyprednisolone | HCID 11047056 | — |
| Reactant | (3-Diazoprop-1-en-2-yl)benzene | HCID 21520875 | — |
| Product | 11beta,17,21-Trihydroxy-16alpha-(2-phenyl-2-propenyloxy)-pregna-1,4-diene-3,20-dione | HCID 68142405 | — |
Reaction Steps
A solution of 1-diazo-2-phenyl-2-propene (prepared from 0.3 mole of N-nitrosourethane precursor) in methanolether at 0° is treated with 11β,16α,17,21-tetrahydroxypregna-1,4-diene-3,20-dione, 16,17-cycloborate (84 mmoles) until nitrogen evolution ceases. Solvent removal gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971773 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-2f60fa2f69f54321895e974f942ef05a |
| Source note | uspto-grants-1976_07 |