反応 #7774

ord-1fdf84e631d54fe4b2045e44440bcbc0

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITAfter 2 h
  2. 2
    濃縮the reaction was concentrated
  3. 3
    workup.ADDITIONEtOAc was added
  4. 4
    洗浄the organic layer was washed with H2O, brine
  5. 5
    その他dried
  6. 6
    ろ過filtered
  7. 7
    濃縮concentrated

実験手順

The above derivative (118ba) (1.96 g) was dissolved in MeOH (15 ml) prior to the addition of 37% formaldehyde in water (1.41 ml). After 10 min, NaBH3CN (708 mg) was added. After 2 h, the reaction was concentrated. EtOAc was added and the organic layer was washed with H2O, brine, dried, filtered, and concentrated to give [(1S,2R,4R)-2-(4-Bromo-benzenesulfonylmethyl)-4-(isopropyl-methyl-amino)-cyclohexyl]-carbamic acid benzyl ester (1.9 g), MS found: (M+H)+=539.3.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087604B2uspto-grants-2006_08