反応 #1697999

ord-af392da56b64444fbf3a07d6f0da0e85

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The catalyst was filtered off
  2. 2
    その他the solvent evaporated
  3. 3
    その他The crude product was purified by flash chromatography

実験手順

3.4 g (9.6 mmol) of 3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine was dissolved in 170 mL MeOH and hydrogenated over 0.30 g Pd(OH)2 at 5 MPa over night. The catalyst was filtered off and the solvent evaporated. The crude product was purified by flash chromatography using MeOH/CH2Cl2, 1/9, followed by MeOH (saturated with NH3 (g))/CH2Cl21 1/9, as eluent to yield 1.2 g (67%) of the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06984627B1uspto-grants-2006_01