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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449482Generated: October 30, 2026

Hydrochloric Acid → HCID 15292241, compound

https://huagongshe.com/reaction/1449482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(3S,5R,8R,9S,10S,13R,14S,17S)-17-[(E)-hydroxyiminomethyl]-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,14-diolHCID 9819105—
SolventMethanolHCID 887—
ProductHCID 15292241HCID 1529224174.6%

Reaction Steps

A stirred solution of 0.60 g of (E)-17β-hydroxyiminomethyl-5β-androstane-3β,14β-diol (prepared following the procedure described in DE 4,227,605 for similar compounds) in 6 ml of methanol was acidified to pH 3 with 1N HCl. 0.30 g of NaBH3CN were added and 0.1N HCl was continuously added, by means of a pH-stat, to maintain pH 2.8+3.0. After 6 hr, 0.15 g of NaBH3CN were added and the reaction was left on stirring overnight. The solution was basified to pH 10 with 2.5N NaOH and methanol was evaporated under reduced pressure. The mixture was extracted with ethyl acetate; the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by flash-chromatography (SiO2) using cyclohexane/ethyl acetate 20/80 as the eluant; the fractions containing the title compound were collected and evaporated to dryness under reduced pressure. The residue was dissolved with diethyl ether/ethyl acetate and the solution was added with the stoichiometric amount of oxalic acid to give 0.45 g of the title compound (I-ah), as a white solid, oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599806
Source datasetuspto-grants-1997_02
ORD IDord-40743b1a76d84af680e5cdf93468e819
Source noteuspto-grants-1997_02