Prednisone → 21-Hydroxypregna-1,4-diene-3,11,20-trione

HRID 982532

반응식

HRID 982532 반응식
C[Si](I)(C)C.O[C@:7]1([C@:28]2([CH3:29])[C@H:14]([C@H:15]3[C@H:25]([C:26](=[O:30])[CH2:27]2)[C@:23]2([CH3:24])[C:18](=[CH:19][C:20](=[O:31])[CH:21]=[CH:22]2)[CH2:17][CH2:16]3)[CH2:13][CH2:12]1)[C:8](=[O:11])[CH2:9][OH:10].S([O-])([O-])=O.[Na+].[Na+]>C(#N)C>[OH:10][CH2:9][C:8](=[O:11])[C@@H:7]1[C@:28]2([CH3:29])[C@H:14]([C@H:15]3[C@H:25]([C:26](=[O:30])[CH2:27]2)[C@:23]2([CH3:24])[C:18](=[CH:19][C:20](=[O:31])[CH:21]=[CH:22]2)[CH2:17][CH2:16]3)[CH2:13][CH2:12]1

참가 물질

5

반응물 3

HCID 5865PrednisoneHCID 24437Sodium SulfiteHCID 85247Trimethylsilyl iodide

생성물 1

HCID 19183721-Hydroxypregna-1,4-diene-3,11,20-trione

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Trimethylsilyl iodide (5.12 ml, 7.20 g, 36.0 mmol) is added dropwise to a solution of 17α,21-dihydroxypregna-1,4-diene-3,11,20-trione (3.23 g) in freshly distilled acetonitrile. After 30 min, sodium sulfite solution (5%, 150 ml) is added to the reaction mixture. The mixture is partitioned with chloroform (400 ml). The phases are separated, and the aqueous phases is extracted twice with chloroform. The organic layers are combined, washed with sodium bicarbonate (5%), saline, dried over sodium sulfate and concentrated. The concentrate is flash chromatographed eluting with ethyl acetate/hexane (2.3/1). The appropriate fractions are pooled to give 21-hydroxypregna-1,4-diene-3,11,20-trione as an oil and 17-epi-21-hydroxypregna-1,4-diene-3,11,20-trione as a solid, mp 203-206°.

후처리

  1. customThe mixture is partitioned with chloroform (400 ml)
  2. customThe phases are separated
  3. extractionthe aqueous phases is extracted twice with chloroform
  4. washwashed with sodium bicarbonate (5%), saline
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated
  7. customchromatographed
  8. washeluting with ethyl acetate/hexane (2.3/1)

출처 및 근거

ORD 기록
ord-31802dc1b3444ae58c4fe595a52864dc
출처 데이터셋
uspto-grants-1991_02
특허 번호
US04996318

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