Diethyl Ether → 1-(5-(1-Aminoethyl)-1-methyl-1H-pyrrolo[3,2-b]pyridin-6-yl)-4-methylpiperidin-4-ol
反応式
[OH:1][C:2]1([CH3:20])[CH2:7][CH2:6][N:5]([C:8]2[CH:9]=[C:10]3[N:18]([CH3:19])[CH:17]=[CH:16][C:11]3=[N:12][C:13]=2[C:14]#[N:15])[CH2:4][CH2:3]1.[CH3:21][Mg]Br.CCOCC.[BH4-].[Na+]>C1COCC1>[NH2:15][CH:14]([C:13]1[N:12]=[C:11]2[CH:16]=[CH:17][N:18]([CH3:19])[C:10]2=[CH:9][C:8]=1[N:5]1[CH2:6][CH2:7][C:2]([CH3:20])([OH:1])[CH2:3][CH2:4]1)[CH3:21]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 0 °C
実験手順
To a solution of 6-(4-hydroxy-4-methylpiperidin-1-yl)-1-methyl-1H-pyrrolo[3,2-b]pyridine-5-carbonitrile (245 mg, 0.906 mmol) in THF (5 mL) at 0° C. was slowly added 3M methylmagnesium bromide in ether (1.21 mL, 3.63 mmol). The resulting yellow solution was stirred at 0° C. for 2.5 hours. The reaction was quenched with MeOH (5 mL) and stirred for 15 minutes at RT. Sodium borohydride (68.6 mg, 1.81 mmol) was added. The reaction was stirred for 1 hour, quenched with 1M HCl (5 mL), and then stirred for an additional 15 minutes. The mixture was subsequently diluted with EtOAc and washed with saturated aqueous NaHCO3 (3×). The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo to give the title compound, which was used without further purification. ESI-MS m/z [M+H]+ calc'd for C16H24N4, 289; found 289.
後処理
- customat 0° C.
- customThe reaction was quenched with MeOH (5 mL)
- stirringstirred for 15 minutes at RT
- stirringThe reaction was stirred for 1 hour
- customquenched with 1M HCl (5 mL)
- stirringstirred for an additional 15 minutes
- additionThe mixture was subsequently diluted with EtOAc
- washwashed with saturated aqueous NaHCO3 (3×)
- dry with materialThe combined organic layers were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-72b9dea6ea1c429bb7dfd511c8b7aadd
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08835420B2
反応ノート
読み込み中…