Sodium Hydroxide → 1-(6-Methylpyrimidin-4-yl)piperidin-4-amine
反応式
Cl.Cl.[CH3:3][C:4]1[N:9]=[CH:8][N:7]=[C:6]([N:10]2[CH2:15][CH2:14][CH:13]([NH2:16])[CH2:12][CH2:11]2)[CH:5]=1.[OH-].[Na+]>C(Cl)Cl>[CH3:3][C:4]1[N:9]=[CH:8][N:7]=[C:6]([N:10]2[CH2:15][CH2:14][CH:13]([NH2:16])[CH2:12][CH2:11]2)[CH:5]=1参加物
4
実験手順
1-(6-Methylpyrimidin-4-yl)piperidin-4-amine dihydrochloride (see example 30b, 2 g, 7.54 mmol) was neutralized with 2 N NaOH solution and CH2Cl2, the aqueous layers were extracted three times with CH2Cl2, the combines organic layers were dried over Na2SO4, filtered and the solvent was evaporated. The title compound was obtained as a brown oil (1.31 g, 90%).
後処理
- extractionthe aqueous layers were extracted three times with CH2Cl2
- dry with materialthe combines organic layers were dried over Na2SO4
- filtrationfiltered
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-d1a97e2157054c4bac830b1e9fca58d2
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08486967B2
反応ノート
読み込み中…