Potassium Carbonate → (R)-(1-(2-(2-Cyclopropylpyrimidin-4-yl)-1H-imidazo[4,5-b]pyrazin-6-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone
反応式
Br[C:2]1[N:7]=[C:6]2[NH:8][C:9]([C:11]3[CH:16]=[CH:15][N:14]=[C:13]([CH:17]4[CH2:19][CH2:18]4)[N:12]=3)=[N:10][C:5]2=[N:4][CH:3]=1.[NH:20]1[CH2:25][CH2:24][CH2:23][C@@H:22]([C:26]([N:28]2[CH2:32][CH2:31][CH2:30][CH2:29]2)=[O:27])[CH2:21]1.C(=O)([O-])[O-].[K+].[K+].[F-].[Cs+]>O.Cl.COCCOCCOC>[CH:17]1([C:13]2[N:12]=[C:11]([C:9]3[NH:8][C:6]4=[N:7][C:2]([N:20]5[CH2:25][CH2:24][CH2:23][C@@H:22]([C:26]([N:28]6[CH2:29][CH2:30][CH2:31][CH2:32]6)=[O:27])[CH2:21]5)=[CH:3][N:4]=[C:5]4[N:10]=3)[CH:16]=[CH:15][N:14]=2)[CH2:19][CH2:18]1参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 150 °C
実験手順
A mixture of 6-bromo-2-(2-cyclopropylpyrimidin-4-yl)-1H-imidazo[4,5-b]pyrazine (86 mg, 0.3 mmol), (R)-piperidin-3-yl(pyrrolidin-1-yl)methanone (95 mg, 0.4 mmol), potassium carbonate (98.4, 0.7 mmol), cesium fluoride (124 mg, 0.8 mmol) and diglyme (1.0 mL) was heated to 150° C. for 3 days. The mixture was diluted with water and aqueous hydrochloric acid (1N). The mixture was extracted with ethyl acetate (3×). The combined organics were washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified via HPLC to afford the title compound. MS (ESI+) (M+H) 419.3, HPLC retention time 2.44 min (Method A).
後処理
- extractionThe mixture was extracted with ethyl acetate (3×)
- washThe combined organics were washed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified via HPLC
出典と根拠
- ORDレコード
- ord-bf44809cecea40d3ae4e5db7d3bdd3e7
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09296745B2
反応ノート
読み込み中…