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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080629Generated: November 4, 2026

Hydrogen Bromide → (3S,5R,8R,9S,10S,13R,14S,17R)-17-[(E,3E)-3-(4,5-dihydro-1H-imidazol-2-ylhydrazinylidene)prop-1-enyl]-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/1080629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2-Hydrazino-delta-2-imidazoline hydrobromideHCID 3085099—
Reactant(E)-3beta,14beta-dihydroxy-5beta-pregn-20-ene-21-carboxaldehydeHCID 10736377—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(3S,5R,8R,9S,10S,13R,14S,17R)-17-[(E,3E)-3-(4,5-dihydro-1H-imidazol-2-ylhydrazinylidene)prop-1-enyl]-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,14-diolHCID 1529261259.9%

Reaction Steps

A solution of 1.19 g of 2-hydrazino-2-imidazoline hydrobromide in 20 ml of water and 60 ml of dioxane was made acid to pH 3 with 0.1N HBr. A solution of 2.08 g of (E)-3β,14β-dihydroxy-5β-pregn-20-ene-21-carboxaldehyde (Fullerton D. S. et al., J. Med. Chem., 1976, 19, 1330) in 25 ml of dioxane was added at room temperature. After 3 days, the solution was evaporated to dryness under reduced pressure. The crude product was purified by flash chromatography (SiO2) using chloroform/methanol/28% ammonium hydroxide 90/10/1 as the eluant; the fractions containing the title compound were collected and evaporated to dryness. The residue was ground with ethyl acetate and ethanol to give 1.54 g of the title compound (I-ac) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583127
Source datasetuspto-grants-1996_12
ORD IDord-1ccbac334e3948bbb594d4eb0e0b0e82
Source noteuspto-grants-1996_12