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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912686Generated: October 30, 2026

HCID 69133284, compound → (6E,8R,9S,10R,13S,14S)-6-hydroxyimino-10,13-dimethyl-1,2,4,5,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione

https://huagongshe.com/reaction/1912686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69133284HCID 69133284—
Reactant(NE)-N-[(2S,5S,6R,14R,15S)-2,6-dimethyl-18,21,22,25-tetraoxahexacyclo[15.4.4.01,17.02,15.05,14.06,11]pentacosan-12-ylidene]hydroxylamineHCID 178421204—
Product(6E,8R,9S,10R,13S,14S)-6-hydroxyimino-10,13-dimethyl-1,2,4,5,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dioneHCID 8765358370%

Reaction Steps

The title compound II-at was prepared in 70% yield from 3,3:17,17-bis(ethylendioxy)-6(E)-hydroxyiminoandrostane by the procedure described above for the preparation of 6α-cyanoandrostane-3,17-dione (II-ac, Prepn. 3). 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 70/30). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 10.61 (s, 1H), 3.29 (dd, 1H), 2.61-1.03 (m, 19H), 0.88 (s, 3H), 0.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609644B2
Source datasetuspto-grants-2013_12
ORD IDord-ac7f6f57f51e4e99915a792bd552a666
Source noteuspto-grants-2013_12