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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726136Generated: October 29, 2026

HCID 67615161, compound → HCID 53807267, compound

https://huagongshe.com/reaction/726136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67615161HCID 67615161—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductHCID 53807267HCID 53807267—

Reaction Steps

A solution of 17β-Hydroxymethyl-3b-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene (prepared as described in Example 5 above), in chloroform (250 mL) is treated with activated manganese(IV) oxide. After stirring 3.5 h, the manganese salts are removed by filtration through Celite. The solution is concentrated and chromatographed on silica gel (50% ethyl acetate/hexanes) to give 17β-hydroxymethyl-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one of sufficient purity to carry on to subsequent steps; yield 9.75 g (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708001
Source datasetuspto-grants-1998_01
ORD IDord-2de128dc3c2644f2acf15e726b3d5ee9
Source noteuspto-grants-1998_01