trans-N-[3-(3-pyridyl)cyclohexyl]phthalimide → trans-3-(3-Pyridyl)cyclohexylamine
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C@H:7]2[CH2:12][CH2:11][CH2:10][C@H:9]([N:13]3C(=O)C4=CC=CC=C4C3=O)[CH2:8]2)[CH:2]=1>CCO>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C@H:7]2[CH2:12][CH2:11][CH2:10][C@H:9]([NH2:13])[CH2:8]2)[CH:2]=1参加物
3
実験手順
A mixture of trans-N-[3-(3-pyridyl)cyclohexyl]phthalimide (3.00 g, 9.79 mmol) and hydrazinemonohydorate (0.95 mL, 19.6 mmol) in EtOH (40 mL) was stirred at room temperature for 1.5 h. The reaction mixture was filtered followed by the removal of solvent. The crude product was purified by column chromatography (NH, EtOAc) to yield trans-3-(3-pyridyl)cyclohexylamine (1.08 g, 60%) as colorless oil.
後処理
- filtrationThe reaction mixture was filtered
- customfollowed by the removal of solvent
- customThe crude product was purified by column chromatography (NH, EtOAc)
出典と根拠
- ORDレコード
- ord-74dd4d4486cf4557ae5649deffc813e6
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08071591B2
反応ノート
読み込み中…