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

HRID 553912
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 553912
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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

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

Produkt 1

HCID 69069771(6R*,9aS*)-6-(2-fluorophenyl)-3-iodooctahydroquinolizin-4-one
Ausbeute 107,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-41a3e33fb252406f93bdb506f751eeee
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08048878B2

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