4-Azetidin-1-yl-1-benzyl-piperidine → 4-(Azetidin-1-YL)piperidine
反応式
[N:1]1([CH:5]2[CH2:10][CH2:9][N:8](CC3C=CC=CC=3)[CH2:7][CH2:6]2)[CH2:4][CH2:3][CH2:2]1.[H][H]>CO.[Pd]>[N:1]1([CH:5]2[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]2)[CH2:4][CH2:3][CH2:2]1参加物
5
実験手順
3.2 g (13.9 mmol) 4-azetidin-1-yl-1-benzyl-piperidine dissolved in 50 mL MeOH were hydrogenated in the autoclave in the presence of 0.5 g Pd/C (10%) at 50° C. and 3 bar hydrogen pressure until the calculated volume of hydrogen had been taken up. The catalyst was filtered off and the solvent was eliminated under reduced pressure.
後処理
- filtrationThe catalyst was filtered off
出典と根拠
- ORDレコード
- ord-a920274d7d824753a91b7afa7bd1fc4f
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700589B2
反応ノート
読み込み中…