反応式
C1(C)C=CC(S(O)(=O)=O)=CC=1.[NH2:12][CH:13]([C:16]#[N:17])[C:14]#[N:15].[CH:18](=[N:22][OH:23])[C:19]([CH3:21])=O>CC(O)C>[NH2:15][C:14]1[C:13]([C:16]#[N:17])=[N:12][C:19]([CH3:21])=[CH:18][N+:22]=1[O-:23]参加物
4
実験手順
Aminomalononitrile p-toluenesulfonate salt (20.0 g, 79 mmol) and pyruvaldehyde 1-oxime (6.88 g, 79 mmol) were combined in a flask. iPrOH (140 mL) was added, and the resulting yellow slurry was allowed to stir at room temperature for 18 h, during which time a yellow precipitate accumulated. The mixture was filtered and the precipitate was washed with iPrOH (2×50 mL) and DI H2O (20 mL), then lyophilized to give 2-amino-3-cyano-5-methypyrazine N-oxide (10.7 g).
後処理
- filtrationThe mixture was filtered
- washthe precipitate was washed with iPrOH (2×50 mL) and DI H2O (20 mL)
出典と根拠
- ORDレコード
- ord-413b1cd18a144742a09ab32d88c2f064
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08093244B2
関連ノート
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