反応式
[Br:1][C:2]1[C:3]([CH3:9])=[N:4][C:5](Cl)=[CH:6][CH:7]=1.[CH3:10][N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:14]2[CH2:15][CH2:16][N:11]([CH3:10])[CH2:12][CH2:13]2)=[N:4][C:3]=1[CH3:9]参加物
4
実験手順
A solution of 3-bromo-6-chloro-2-methylpyridine (700 mg, 3.39 mmol) and 1-methylpiperazine (0.753 mL, 6.78 mmol) in DMF (4 mL) was heated in microwave reactor at 150° C. for 50 minutes. The mixture was subsequently purified via preparative HPLC, eluting with a gradient of 10-70% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA) to give the title compound.
後処理
- customThe mixture was subsequently purified via preparative HPLC
- washeluting with a gradient of 10-70% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA)
出典と根拠
- ORDレコード
- ord-06e1793c54df47aa974c0aa09112478d
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434743B2
関連ノート
読み込み中…