Reaktion #42101

ord-735b7ed88fb94323b68b01653e9c3a81

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter 1 hour 45 minutes the reaction was quenched with 2 M aqueous HCl
  2. 2
    workup.ADDITIONdiluted with EtOAc
  3. 3
    Waschenwashed with saturated aqueous NaHCO3 solution
  4. 4
    EinengenThe dried solution (Na2SO4) was concentrated
  5. 5
    Sonstigepurified via flash chromatography on silica gel
  6. 6
    Wascheneluted with 20% EtOAc in hexane affording the title compound

Vorschrift

To 6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-2-(isobutylamino)pyridine-3-carbonitrile [prepared by reacting the product of Example 1 step C with isobutyl amine] (0.26 g) in TH (2.5 mL) was added MeMgBr (0.47 mL, 1.4 M solution in toluene THF 3:1) followed by propionyl chloride. After 1 hour 45 minutes the reaction was quenched with 2 M aqueous HCl, diluted with EtOAc and washed with saturated aqueous NaHCO3 solution. The dried solution (Na2SO4) was concentrated and purified via flash chromatography on silica gel eluted with 20% EtOAc in hexane affording the title compound. HPLC/MS: 486.2(M+1), 488.2 (M+3); Rt=4.60 min.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728141B2uspto-grants-2010_06