反応式
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[N:5]2[N:9]=[CH:10][CH:11]=[C:4]2[N:3]=1.[NH4+:12].[OH-]>>[Cl:1][C:2]1[CH:7]=[C:6]([NH2:12])[N:5]2[N:9]=[CH:10][CH:11]=[C:4]2[N:3]=1参加物
3
反応条件
- 温度
- 85 °C
実験手順
To 5,7-dichloropyrazolo[1,5-a]pyrimidine (7.6 g, 40.4 mmol) in a sealed vessel was added NH4OH (100 mL). The vessel was then sealed and heated at 85° C. for 2.5 hours, at which time the consistency of the white solid had changed (from foamy white solid to free-flowing white solid). The vessel was removed from the heat source and allowed to cool to room temperature overnight. On cooling, the contents of the vessel were collected and dried by vacuum filtration giving 5-chloropyrazolo[1,5-a]pyrimidin-7-amine as a yellow-tinged white solid (6.8 g).
後処理
- customThe vessel was then sealed
- customThe vessel was removed from the heat source
- temperatureto cool to room temperature overnight
- temperatureOn cooling
- customthe contents of the vessel were collected
- customdried by vacuum filtration
出典と根拠
- ORDレコード
- ord-62ddcfe51f8a41c18e1c5170c8284292
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09227971B2
関連ノート
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