Methyl iodide → 4-Bromo-1,3,5-trimethylpyrazole
반응식
[Br:1][C:2]1[C:3]([CH3:8])=[N:4][NH:5][C:6]=1[CH3:7].[H-].[Na+].[H][H].IC.[C:15](=O)([O-])O.[Na+]>CN(C)C=O>[Br:1][C:2]1[C:3]([CH3:8])=[N:4][N:5]([CH3:15])[C:6]=1[CH3:7]참가 물질
7
실험 절차
4-Bromo-3,5-dimethylpyrazole (10 g) in dry dimethylformamide (50 ml) was added to a stirred suspension of sodium hydride (1.8 g) in dry dimethylformamide at 0° C. When the evolution of hydrogen was complete, iodomethane (8.9 g) was added dropwise. The mixture was allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate (5 ml) was added. Following evaporation under high vacuum, the residue was purified by column chromatography to give the title compound.
후처리
- additionwas added
- customevaporation under high vacuum
- customthe residue was purified by column chromatography
출처 및 근거
- ORD 기록
- ord-ac7f5eb35ef547d1a557dea38319f19e
- 출처 데이터셋
- uspto-grants-1998_03
- 특허 번호
- US05731335
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