HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67536381, compound → (7E,8R,9S,10S,13S,14S)-10,13-dimethyl-7-prop-2-enoxyimino-1,2,4,5,6,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67536381 | HCID 67536381 | — |
| Reactant | HCID 178460000 | HCID 178460000 | — |
| Product | (7E,8R,9S,10S,13S,14S)-10,13-dimethyl-7-prop-2-enoxyimino-1,2,4,5,6,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione | HCID 87655215 | 76% |
Reaction Steps
The title compound II-av was prepared in 76% yield from 3,3:17,17-bis(ethylendioxy)-7-(E)-allyloxyiminoandrostane by the procedure described above for the preparation of 6-methyleneandrostane-3,17-dione (II-ac, Prepn. 13). The crude product was purified by flash chromatography (SiO2, n-hexane/EtOAc 8/2). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 5.98 (1H, m), 5.24 (1H, m), 5.14 (1H, m), 4.48 (2H, m), 2.40-1.10 (20H, m), 1.00 (3H, s), 0.81 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536160B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-b09563a52f92484382a41836d55413b4 |
| Source note | uspto-grants-2013_09 |