反応式
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[NH:7][NH2:8].[F:9][CH:10]([F:19])[C:11]([O:13][C:14](=[O:18])[CH:15]([F:17])[F:16])=[O:12]>>[F:9][CH:10]([F:19])[C:11]([OH:13])=[O:12].[F:17][CH:15]([F:16])[C:14]([NH:8][NH:7][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][N:1]=1)=[O:18]参加物
3
実験手順
Pyrazin-2-yl-hydrazine 23a (1 g, 9 mmol) was added in an eggplant-shaped bottle (25 mL), followed by dropwise addition of difluoroacetic anhydride (4 g, 22.98 mmol) at 0° C. After stirring at room temperature for 3 hours, the reaction mixture was concentrated under reduced pressure to obtain crude 2,2-difluoro-N′-pyrazin-2-yl-acetohydrazide difluoroacetate 23b (2 g) as a brown oil. The product was used directly in the next reaction without purification.
後処理
- concentrationthe reaction mixture was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-08c3e720c3cb4b559ddc63c6d6bcdd93
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09273052B2
関連ノート
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