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HRID 1003233作成日:2026年10月26日

Dehydroepiandrosterone → Dehydroepiandrosterone

https://huagongshe.com/reaction/1003233

反応式

関与物質

役割名称HCID仕込み量
反応物DehydroepiandrosteroneHCID 5881—
反応物22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONEHCID 69625815—
生成物DehydroepiandrosteroneHCID 5881—
生成物HCID 178420941HCID 178420941—

反応手順

The synthesis of 22,29-epoxy-3,29-dihydroxy-14,-stigmastan-15-one (260) can be accomplished in ten steps from dehydroisoandrosterone (247). Catalytic hydrogenation of the Δ5 carbon-carbon double bond in compound 247 yields compound 250, which contains a trans-fused A/B ring-system. Compound 247 is dissolved in EtOAc and 10% Pd/C is added. The mixture is stirred under H2 at room temperature overnight. Filtration through celite and concentration yields compound 250, which can be used directly in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06046185
出典データセットuspto-grants-2000_04
ORD IDord-8f631006734d4e3a8529b1bee669ef6f
出典メモuspto-grants-2000_04