반응 #168410

ord-ce1f59970cb64815844736d4f2dd8773

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Then reaction
  2. 2
    기타quenched with aqueous saturated NaHCO3 solution (40 mL)
  3. 3
    추출extracted with dichloromethane (2×30 mL)
  4. 4
    세척The combined organic extracts were washed with brine (10 mL)
  5. 5
    건조dried over anhydrous Na2SO4
  6. 6
    여과filtered
  7. 7
    농축concentrated
  8. 8
    기타Purification of the residue on a silica gel column (0 to 100% EtOAc/hexanes)

실험 절차

To a stirred solution of {6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridin-2-yl}(3-fluoropyridin-2-yl)methanol (807 mg, 1.61 mmol) in dichloromethane (15 mL) was added Dess-Martin periodinane (2.7 g, 6.45 mmoL) at 0° C. Then reaction was gradually warmed to room temperature and stirred for 2 hours. The reaction mixture was diluted with dichloromethane (15 mL), quenched with aqueous saturated NaHCO3 solution (40 mL), and extracted with dichloromethane (2×30 mL). The combined organic extracts were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered, and concentrated. Purification of the residue on a silica gel column (0 to 100% EtOAc/hexanes) afforded {6-chloro-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-d]pyridin-2-yl}(3-fluoropyridin-2-yl)methanone. MS APCl calcd. for C25H22Cl2FN5O [M+H]+ 498. found 498.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846657B2uspto-grants-2014_09