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Iodine → (6R*,9aS*)-6-(2-fluorophenyl)-3-iodooctahydroquinolizin-4-one

HRID 553912
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HRID 553912 반응식
I[Si](C)(C)C.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C@H:13]1[CH2:22][CH2:21][CH2:20][C@@H:19]2[N:14]1[C:15](=[O:23])[CH2:16][CH2:17][CH2:18]2.CN(C)CCN(C)C.[I:32]I.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)Cl.C(OCC)(=O)C>[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C@H:13]1[CH2:22][CH2:21][CH2:20][C@@H:19]2[N:14]1[C:15](=[O:23])[CH:16]([I:32])[CH2:17][CH2:18]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 807IodineHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 24477Sodium ThiosulfateHCID 85247Trimethylsilyl iodideHCID 69077331(6R*,9aS*)-6-(2-fluorophenyl)octahydroquinolizin-4-one

생성물 1

HCID 69069771(6R*,9aS*)-6-(2-fluorophenyl)-3-iodooctahydroquinolizin-4-one수율 107.2%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

실험 절차

Iodotrimethylsilane (0.28 mL) was added to a solution of (6R*,9aS*)-6-(2-fluorophenyl)octahydroquinolizin-4-one (309 mg) and N,N,N′,N′-tetramethylethylenediamine (0.66 mL) in methylene chloride (12 mL) under ice-cooling in a nitrogen atmosphere, and the reaction solution was stirred under ice-cooling for 30 minutes. Iodine (476 mg) was added to the reaction solution under ice-cooling, and the reaction solution was stirred under ice-cooling for one hour. Ethyl acetate and a saturated sodium thiosulfate solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 500 mg of the title compound. The property value of the compound is as follows.

후처리

  1. temperaturecooling in a nitrogen atmosphere
  2. temperaturecooling for 30 minutes
  3. temperaturecooling
  4. stirringthe reaction solution was stirred under ice-
  5. temperaturecooling for one hour
  6. customthe organic layer was separated
  7. washThe resulting organic layer was washed with brine
  8. dry with materialdried over magnesium sulfate
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-41a3e33fb252406f93bdb506f751eeee
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08048878B2

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