Reaktion #497389

ord-c41163c66a2046fe8407559eb8c2eba2

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted (2×) with DCM
  2. 2
    Waschenwashed (2×) with an aqueous saturated solution of sodium bicarbonate
  3. 3
    TrocknenThe organic layer was then dried with sodium sulfate
  4. 4
    Sonstigepurified by column chromatography on silica gel using a gradient of 30 to 80% EtOAc in hexanes

Vorschrift

A solution of (1H-benzo[d]imidazol-2-yl)(4-(3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)methanone (0.350 g, 0.881 mmol) in DMF (5 mL) was treated with iodomethane (0.083 mL, 1.321 mmol). The mixture was stirred at RT and after 4 hours, it was diluted with water and extracted (2×) with DCM. The organic portions were combined and washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was then dried with sodium sulfate, reduced and purified by column chromatography on silica gel using a gradient of 30 to 80% EtOAc in hexanes to afford (4-(3-(3,6-dihydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)(1-methyl-1H-benzo[d]imidazol-2-yl)methanone as white solid. MS (ESI, pos. ion) m/z: 411.9 (M+1). IC50 (uM) +++++.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08759532B2uspto-grants-2014_06