Reaktion #40554
ord-bb9f641574f3407fbcc52c5df3b9224e
Reaktionsgleichung
6-Chloro-4-[6-trifluormethyl-1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2-(2-trimethylsilanylethoxymethyl)-2H-pyridazin-3-one
bis(pinacolato)diboron
potassium acetate
→
6-Oxo-5-[6-tri-fluoromethyl-1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-1-(2-trimethylsilanylethoxymethyl)-1,6-dihydropyridazine-3-boronic acid
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
95°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe solution is degassed with argon
- 2FiltrationThe reaction solution is filtered through silica gel
- 3Waschenthe latter is washed with dichloromethane
- 4SonstigeThe solvent is removed in a rotary evaporator
- 5Sonstigethe crude product is purified by RP-HPLC (0-100% acetonitrile in water (+0.01% trifluoroacetic acid))
Vorschrift
6-Chloro-4-[6-trifluormethyl-1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2-(2-trimethylsilanylethoxymethyl)-2H-pyridazin-3-one (prepared in analogy to example 15b), bis(pinacolato)diboron, (1,1′-bis(diphenylphosphine)ferrocene)-palladium(II) chloride-dichloromethane complex and potassium acetate are dissolved in DMSO. The solution is degassed with argon and heated at 95° C. for 2.5 hours. The reaction solution is filtered through silica gel, and the latter is washed with dichloromethane. The solvent is removed in a rotary evaporator, and the crude product is purified by RP-HPLC (0-100% acetonitrile in water (+0.01% trifluoroacetic acid)). MS (ES+) m/z 585 (M+H).