反応 #42101

ord-735b7ed88fb94323b68b01653e9c3a81

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After 1 hour 45 minutes the reaction was quenched with 2 M aqueous HCl
  2. 2
    workup.ADDITIONdiluted with EtOAc
  3. 3
    洗浄washed with saturated aqueous NaHCO3 solution
  4. 4
    濃縮The dried solution (Na2SO4) was concentrated
  5. 5
    その他purified via flash chromatography on silica gel
  6. 6
    洗浄eluted with 20% EtOAc in hexane affording the title compound

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07728141B2uspto-grants-2010_06