反応 #450405

ord-d360addd55cb444a947a2337aca7503a

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITAfter 4 hours
  2. 2
    その他partition the reaction mixture between ethyl acetate and 5% sodium bicarbonate solution
  3. 3
    乾燥Dry the organic layer over Na2SO4
  4. 4
    ろ過filter
  5. 5
    その他evaporate invacuo
  6. 6
    その他to give a residue

実験手順

Add a solution of (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine (1.1 g, 3.1 mmol) in dichloromethane (2 mL) to trifluoromethanesulfonic acid (1.2 mL). After 2.5 hours, add trifluoromethanesulfonic acid (1.2 mL). After 4 hours, partition the reaction mixture between ethyl acetate and 5% sodium bicarbonate solution. Dry the organic layer over Na2SO4, filter, and evaporate invacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% ethyl acetate/hexane and then 25% ethyl acetate/hexane to give the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05872251uspto-grants-1999_02