反応 #42101
ord-735b7ed88fb94323b68b01653e9c3a81
反応方程式
反応物
試薬
なし
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他After 1 hour 45 minutes the reaction was quenched with 2 M aqueous HCl
- 2workup.ADDITIONdiluted with EtOAc
- 3洗浄washed with saturated aqueous NaHCO3 solution
- 4濃縮The dried solution (Na2SO4) was concentrated
- 5その他purified via flash chromatography on silica gel
- 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.