Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][N:8]=[CH:7]2.S(OC)(O[CH3:15])(=O)=O>C1(C)C=CC=CC=1>[Br:1][C:2]1[C:10]2[C:6](=[CH:7][N:8]([CH3:15])[N:9]=2)[CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 7-bromo-1H-indazole (3; 1.71 g, 8.67 mmol) and dimethyl sulfate (0.90 mL, 9.5 mmol) in 30 mL of toluene was stirred at 110° C. for 4 h, then allowed to cool. The mixture was carefully washed with 30 mL of a saturated aqueous NaHCO3 solution, dried over MgSO4, filtered (rinsing with diethyl ether), and concentrated to an orange oil Column chromatography (0→50% EtOAc/hexanes) afforded 7-bromo-2-methyl-2H-indazole (6: R=Me; 1.33 g, 73%) as a light tan solid.
Aufarbeitung
- temperatureto cool
- washThe mixture was carefully washed with 30 mL of a saturated aqueous NaHCO3 solution
- dry with materialdried over MgSO4
- filtrationfiltered
- wash(rinsing with diethyl ether)
- concentrationconcentrated to an orange oil Column chromatography (0→50% EtOAc/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-5bcfa2faa1864037a7c56f18f17778b1
- Quelldatensatz
- uspto-grants-2008_04
- Patentnummer
- US07365211B2
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