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

HRID 553906ノート

反応式

HRID 553906 の反応式
I[Si](C)(C)C.[F:6][C:7]1[CH:8]=[C:9]([C@H:13]2[CH2:22][CH2:21][CH2:20][C@@H:19]3[N:14]2[C:15](=[O:23])[CH2:16][CH2:17][CH2:18]3)[CH:10]=[CH:11][CH:12]=1.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:8]=[C:9]([C@H:13]2[CH2:22][CH2:21][CH2:20][C@@H:19]3[N:14]2[C:15](=[O:23])[CH:16]([I:32])[CH2:17][CH2:18]3)[CH:10]=[CH:11][CH:12]=1

参加物

8

実験手順

Iodotrimethylsilane (0.34 mL) was added to a solution of (6R*,9aS*)-6-(3-fluorophenyl) octahydroquinolizin-4-one (383 mg) and N,N,N′,N′-tetramethylethylenediamine (0.82 mL) in methylene chloride (15 mL) under ice-cooling in a nitrogen atmosphere, and the reaction solution was stirred under ice-cooling for 30 minutes. Iodine (590 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 597 mg of the title compound. The property value of the compound is as follows.

後処理

  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

出典と根拠

ORDレコード
ord-ad84cbae4c9a420282e4f6bafe4bb616
出典データセット
uspto-grants-2011_11
特許番号
US08048878B2

反応ノート

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