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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65403생성일: 2026년 10월 24일

Dexamethasone → Dexamethasone 9,11-epoxide

https://huagongshe.com/ko/reaction/65403

반응식

참여 물질

역할이름HCID투입량
반응물DexamethasoneHCID 5743—
반응물17beta-Hydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dioneHCID 13578837—
생성물Dexamethasone 9,11-epoxideHCID 11143226—

반응 단계

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 (VI) 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614621
출처 데이터셋uspto-grants-1986_09
ORD IDord-4462328e288a41b88b3174407a5f3ed7
출처 메모uspto-grants-1986_09