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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840185Generated: October 30, 2026

HCID 12149919, compound → HCID 70145734, compound

https://huagongshe.com/reaction/840185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12149919HCID 12149919—
ReactantHCID 178435160HCID 178435160—
ReactantHCID 178461633HCID 178461633—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70145734HCID 70145734—

Reaction Conditions

Temperature-22 °C

Reaction Steps

Cuprous chloride (CuCl, 0.7611 g, 7.689 mmol) is slurried in THF (40 mL) under nitrogen and then chilled to −22° C. with a dry ice/tetrachloroethylene bath. Ethylmagnesium chloride solution (2.00 M in ether; 22.0 mL, 44.0 mmol) is added to the cold cuprous chloride slurry and the dark solution is stirred for 90 minutes. A solution of 3β-t-butyldimethylsilyloxy-androst-5,15-dien-17-one (from Example 28C;) in THF (50 mL) is added dropwise via polyethylene cannula to the organometallic solution over 10 minutes, followed by a THF rinse (20 mL). The reaction mixture is stirred for 2 hours at −22° C. and then allowed to warm to ambient temperature over 30 minutes, followed by addition of saturated aqueous NH4Cl (50 mL). The biphasic mixture is extracted with EtOAc (2×40 mL) and the combined organic layers are washed with brine (50 mL), dried over MgSO4, filtered and evaporated to dryness. Purification by flash chromatography gives 15β-ethyl-3β-t-butyldimethylsilyloxy-androst-5-en-17-one, which is deprotected as in Example 19C to give the corresponding 3-alcohol, which is then oxidized as in Example 16D to obtain the title compound, which has the following formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365597B1
Source datasetuspto-grants-2002_04
ORD IDord-64af345b7a694fa79e0b3b44618d1e68
Source noteuspto-grants-2002_04