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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735738Generated: November 2, 2026

1,1-Dimethylhydrazine → (3S,5R,8R,9S,10S,13R,14S,17S)-17-[(E)-(dimethylhydrazinylidene)methyl]-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,14-diol

https://huagongshe.com/reaction/1735738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DimethylhydrazineHCID 5976—
ReactantSodium BicarbonateHCID 516892—
Reactant3beta,14beta-Dihydroxy-5beta-androstane-17beta-carboxaldehydeHCID 10903304—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(3S,5R,8R,9S,10S,13R,14S,17S)-17-[(E)-(dimethylhydrazinylidene)methyl]-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,14-diolHCID 88124783—

Reaction Steps

To a solution of 0.80 g of NaH2PO4.H2O, 1.70 g of Na2HPO4.12H2O and 0.12 ml of N,N-dimethylhydrazine in 200 ml of water a solution of 0.64 g of 3β,14β-dihydroxy-5β-androstane-17β-carboxaldehyde (Boutagy J. and Thomas R., Aust. J. Chem., 1971, 24, 2723) in 20 ml of dioxane was added dropwise at room temperature. After 1.5 hrs the solution was alkalinized with an acqueous solution of NaHCO3 and extracted with ethyl acetate; the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness. The crude product was purified by flash-chromatography (SiO2) using cyclohexane/chloroform/acetone 4/3/3 as eluant to give 0.37 g of the title compound (I-ai), as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538960
Source datasetuspto-grants-1996_07
ORD IDord-3c381e1a763a4967ab4a7b99e58839aa
Source noteuspto-grants-1996_07