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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370413Erstellt: 24. Oktober 2026

Dexamethasone → Dexamethasone 9,11-epoxide

https://huagongshe.com/de/reaction/370413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDexamethasoneHCID 5743—
Edukt17beta-Hydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dioneHCID 13578837—
ProduktDexamethasone 9,11-epoxideHCID 11143226—

Reaktionsschritte

Dexamethasone (9α-fluoro-11β,17α,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione) can also be prepared from 17β-hydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dione by first transforming it to 17α,21-dihydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dione 21-acetate as described above and next transforming it to 17α,21-dihydroxy-16α-methylpregna-1,4,9(11)-triene-3,20-dione 21-acetate by the process of U.S. Pat. No. 3,130,209. 17α,21-Dihydroxy-16α-methylpregna-1,4,9(11)-triene-3,20-dione 21-acetate is then epoxidized by means well known to those skilled in the art, see for example U.S. Pat. No. 3,980,778, Examples 2 and 7 to produce 9β,11β-epoxy-17α,21-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione which is transformed to dexamethasone 21-acetate by the process of U.S. Pat. No. 3,007,932, Example 2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04526720
Quelldatensatzuspto-grants-1985_07
ORD IDord-bb5fd5e14b334bf9a93e97cb5597a1fa
Quellennotizuspto-grants-1985_07