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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735736Generated: November 3, 2026

3beta,14beta-Dihydroxy-5beta-androstane-17beta-carboxaldehyde → HCID 178483809, compound

https://huagongshe.com/reaction/1735736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3beta,14beta-Dihydroxy-5beta-androstane-17beta-carboxaldehydeHCID 10903304—
ReactantHCID 178483810HCID 178483810—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178483809HCID 17848380914.3%

Reaction Steps

To a solution of 0.64 g of 1-amino-3-(2-dimethylaminoethyl)guanidine hydroiodide (prepared following the procedure described in Houben-Weil, Metoden der Organischen Chemie, Band VIII, page 183) in 20 ml of 10-4M hydrochloric acid a solution of 1.10 g of 3β,14β-dihydroxy-5β-androstane-17β-carboxaldehyde (Boutagy J. and Thomas R., Aust. J. Chem., 1971, 24, 2723) in 25 ml of dioxane was added dropwise at room temperature. After 3 hrs, the solution was evaporated to dryness under reduced pressure. The crude product was purified by flash-chromatography (SiO2) using chloroform/methanol/28% ammonium hydroxide 78/20/2 as eluant; the fractions containing the title compound were collected and evaporated to dryness. The residue was ground with di-iso-propyl ether to give 0.15 g of the title compound (I-ag) as hydroiodide, white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538960
Source datasetuspto-grants-1996_07
ORD IDord-6f0f5a360baf4488ba679f750fbb5a35
Source noteuspto-grants-1996_07