反応式
[Cl-].C([Al+]CC)C.[Br:7][C:8]1[N:9]=[C:10]2[CH:16]=[CH:15][NH:14][C:11]2=[N:12][CH:13]=1.[CH3:17][C:18]([CH3:25])([CH2:22][CH:23]=[CH2:24])[C:19](Cl)=[O:20].C([O-])(O)=O.[Na+]>ClCCl>[Br:7][C:8]1[N:9]=[C:10]2[C:16]([C:19](=[O:20])[C:18]([CH3:25])([CH3:17])[CH2:22][CH:23]=[CH2:24])=[CH:15][NH:14][C:11]2=[N:12][CH:13]=1参加物
反応条件
- 温度
- 2.5 °C
実験手順
Diethylaluminum chloride (1.0 M in CH2Cl2, 23.4 mL, 23.4 mmol) was added to a 0-5° C. mixture of 2-bromo-5H-pyrrolo[2,3-b]pyrazine (1.55 g, 7.80 mmol) and 30 mL of dichloromethane in a sealed tube, and the mixture was stirred at 0-5° C. for 20 min. The solution of crude 2,2-dimethyl-4-pentenoyl chloride prepared in the previous step was added dropwise. The resulting mixture was stirred at 60° C. for 64 h, then cooled to 0-5° C. A sat. aq. NaHCO3 solution (50 mL) was carefully added, and the mixture was extracted with three 100 mL portions of ethyl acetate. The combined organic layers were dried over MgSO4, filtered and concentrated to a residue. Column chromatography (0→50% EtOAc/hexanes) afforded 1.033 g (43%) of impure 1-(2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-2,2-dimethyl-pent-4-en-1-one as a brown solid, which was used without further purification. The major impurity is s.m. (typically 15-30% of the mixture).
後処理
- additionwas added dropwise
- stirringThe resulting mixture was stirred at 60° C. for 64 h
- temperaturecooled to 0-5° C
- extractionthe mixture was extracted with three 100 mL portions of ethyl acetate
- dry with materialThe combined organic layers were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated to a residue
出典と根拠
- ORDレコード
- ord-223468fec13a435980aeff76d065aeb0
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US08008298B2
関連ノート
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