反応式
Br[C:2]1[N:7]=[C:6]2[N:8]([C@H:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH3:13])[C:9]([OH:11])=[N:10][C:5]2=[N:4][CH:3]=1.[CH:20](/B(O)O)=[CH:21]/[CH3:22]>>[C:14]1([C@@H:12]([N:8]2[C:6]3=[N:7][C:2](/[CH:20]=[CH:21]\[CH3:22])=[CH:3][N:4]=[C:5]3[N:10]=[C:9]2[OH:11])[CH3:13])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1参加物
反応条件
- 温度
- 90 °C
実験手順
A scintillation vial equipped with a stirbar was charged with (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2-ol (1.0 equiv), (Z)-prop-1-enyl boronic acid (2.0 equiv) and (DPPF)PdCl2 (0.10 equiv). The vial was fitted with a septum-lined cap and purged with nitrogen for 5-10 min. To this mixture was added dioxane (16.6 volume equivalents) and degassed 2N K2CO3 (4.2 volume equivalents) by syringe. The resulting mixture was heated to 90° C. overnight. The mixture was cooled to room temperature, diluted with EtOAc, washed with twice with saturated aq. NaHCO3, and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Biotage MPLC 5%-40% EtOAc/Hexanes) provided the title compound (63%) as an off-white foam. LCMS m/z (APCI)=281.1 (M+H).
後処理
- customA scintillation vial equipped with a stirbar
- customThe vial was fitted with a septum-lined
- customcap
- custompurged with nitrogen for 5-10 min
- additionTo this mixture was added dioxane (16.6 volume equivalents)
- customdegassed 2N K2CO3 (4.2 volume equivalents) by syringe
- temperatureThe mixture was cooled to room temperature
- additiondiluted with EtOAc
- washwashed with twice with saturated aq. NaHCO3
- dry with materialThe organic layer was dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-cada75ad2ad64e5fae809388d65267b8
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08716291B2
関連ノート
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