1-Bromo-2-methylpropane → 1-Isobutyl-5-methoxy-1H-indazole

HRID 2112212Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2112212
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][N:7]=[CH:6]2.C([O-])([O-])=O.[K+].[K+].Br[CH2:19][CH:20]([CH3:22])[CH3:21]>CN(C=O)C>[CH2:19]([N:8]1[C:9]2[C:5](=[CH:4][C:3]([O:2][CH3:1])=[CH:11][CH:10]=2)[CH:6]=[N:7]1)[CH:20]([CH3:22])[CH3:21]

Komponenten

5

Edukt 3

HCID 65551-Bromo-2-methylpropane2×HCID 11430Potassium CarbonateHCID 133468605-Methoxy-1H-indazole

Produkt 1

HCID 574187691-Isobutyl-5-methoxy-1H-indazoleAusbeute 36,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A solution of 5-methoxy-1H-indazole (5.00 g, 33.7 mmol) in DMF (100 mL) was treated with K2CO3 (5.83 g, 42.2 mmol) and stirred at room temperature for 15 minutes. To this solution was added 1-bromo-2-methylpropane (5.09 g, 37.1 mmol) and the resulting mixture was heated to 110° C. for 18 hours. Another equivalent of 1-bromo-2-methyl-propane was added and the mixture continued to heat for 48 hours more. The mixture was concentrated under reduced pressure and dissolved in dichloromethane. The solution was washed with 1N HCl, filtered, and concentrated under reduced pressure. The residue was chromatographed on Biotage eluting with hexanes/ether (5:1) to afford 2.51 g of orange oil (36% yield).

Aufarbeitung

  1. temperaturethe resulting mixture was heated to 110° C. for 18 hours
  2. temperatureto heat for 48 hours more
  3. concentrationThe mixture was concentrated under reduced pressure
  4. dissolutiondissolved in dichloromethane
  5. washThe solution was washed with 1N HCl
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was chromatographed on Biotage
  9. washeluting with hexanes/ether (5:1)

Quellen und Nachweise

ORD-Eintrag
ord-9a0f4434189a4510a907475eb115043a
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07521447B2

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