反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=O)[CH:5]=[N:6][CH:7]=1.[NH:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[CH:5]=[N:6][CH:7]=1参加物
3
実験手順
The title compound was prepared in a similar way as described in Example 18, Step C, using 5-bromo-pyridine-3-carbaldehyde and morpholine. The crude compound was purified (SiO2: 0-3% 2 M NH3 in MeOH/DCM) to provide the title compound (61%).
後処理
- customThe title compound was prepared in a similar way
- customThe crude compound was purified (SiO2: 0-3% 2 M NH3 in MeOH/DCM)
出典と根拠
- ORDレコード
- ord-fa162b65c69e4dc3b185bf027fd7d8b4
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423147B2
関連ノート
読み込み中…