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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42106Generated: October 30, 2026

HCID 67536381, compound → (5R,6E,8R,9S,10R,13S,14S)-5-hydroxy-6-methoxyimino-10,13-dimethyl-2,4,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione

https://huagongshe.com/reaction/42106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67536381HCID 67536381—
ReactantHCID 154041432HCID 154041432—
Product(5R,6E,8R,9S,10R,13S,14S)-5-hydroxy-6-methoxyimino-10,13-dimethyl-2,4,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dioneHCID 8765545480%

Reaction Steps

The title compound II-ar was prepared in 80% yield from 3,3:17,17-bis(ethylendioxy)-5α-hydroxy-6-(E)-methoxyiminoandrostane by the procedure described above for the preparation of 6-methyleneandrostane-3,17-dione (II-ac, Prepn. 13). The combined organic extracts were washed with H2O, dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (SiO2, n-hexane/acetone/CH2Cl2 60/20/20). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 5.46 (1H, s), 3.75 (3H, s), 3.20-2.93 (1H, dd), 2.86-2.75 (1H, d), 2.30-1.10 (17H, m), 0.96 (3H, s), 0.77 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536160B2
Source datasetuspto-grants-2013_09
ORD IDord-d3988ce5b8ba42909d0a853d2ac79ab5
Source noteuspto-grants-2013_09