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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582517Generated: October 25, 2026

Water → 3alpha-Hydroxy-21-(pyrid-3-yl)oxy-5beta-pregnan-20-one

https://huagongshe.com/reaction/582517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium CarbonateHCID 11430—
Reactant21-Bromo-3alpha-hydroxy-5beta-pregnan-20-oneHCID 86754251—
SolventDimethylformamideHCID 6228—
Product3alpha-Hydroxy-21-(pyrid-3-yl)oxy-5beta-pregnan-20-oneHCID 2131032016%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 3α-hydroxy-21-bromo-5β-pregnan-20-one-(300 mg, 0.76 mmol) in DMF (5 mL) was added 3-hydroxypyridine (215 mg, 2.27 mmol) and K2CO3 (313 mg, 2.27 mmol) and the mixture obtained was stirred at 25° C. for 0.5 h. The reaction mixture was then poured into a separatory funnel containing water (30 mL) and the mixture was extracted with EtOAc (3×35 mL). The combined extracts were washed with water (2×25 mL) and then dried over Na2SO4. Removal of the solvent in vacuo resulted in the crude product which was purified by flash chromatography over silica gel to yield the pure 3α-hydroxy-21-(pyrid-3-yl)oxy-5β-pregnan-20-one (50 mg); mp 63-66° C.; TLC Rf (MeOH:CH2Cl2 5:95)=0.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925630
Source datasetuspto-grants-1999_07
ORD IDord-714c4f144bb049db916719f6a39df0f5
Source noteuspto-grants-1999_07