反応 #651265

ord-cf4bd56af3f6478480e28e43ea6cc2eb

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The precipitate is collected
  2. 2
    その他dried
  3. 3
    その他is used without further purification in the next step

実験手順

To 8.05 g (40.0 mmol) 4-benzyloxy-1H-pyridin-2-one in 50 mL THF is added at 0° C. subsequently 4.94 g (44.0 mmol) potassium tert-butylate, 739 mg (2.00 mmol) tert-butyl ammonium-iodide and 15.3 g (48.0 mmol) 1-[7-(2-chloro-acetyl)-1,2,4,5-tetrahydro-3-benzazepin-3-yl]-2,2,2-trifluoro-ethanone. The reaction mixture is stirred overnight at RT and poured onto 500 mL water. 100 ml tert-butylmethylether is added. The precipitate is collected and dried. The product, which contains 20% 1-[7-(2-chloro-acetyl)-1,2,4,5-tetrahydro-3-benzazepin-3-yl]-2,2,2-trifluoro-ethanone is used without further purification in the next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08067590B2uspto-grants-2011_11