反応 #85075

ord-7aa98a07968c40c28c18062ce527e6a4

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The crude product was purified by preparative HPLC [column
  2. 2
    その他a further 3 min 90% acetonitrile

実験手順

97.0 mg (253 μmol) of 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4,4-difluorobutanoic acid (racemate), 42.0 mg (253 μmol) of ethyl 4-aminobenzoate, 36.0 mg (253 μmol) of Oxima and 39.0 μl (253 μmol) of DIC in 2.5 ml of dimethylformamide were reacted according to General Method 5B. The crude product was purified by preparative HPLC [column: Chromatorex C18, 10 μm, 125×30 mm, mobile phase: acetonitrile/0.05% formic acid gradient (0 to 3 min 10% acetonitrile, to 35 min 90% acetonitrile and a further 3 min 90% acetonitrile)]. Yield: 81.7 mg (60% of theory)

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09434690B2uspto-grants-2016_09