反応式
[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH:13]([F:15])[F:14])[NH:6]2.Br[CH:17]([CH3:21])[C:18]([NH2:20])=[O:19].C([O-])([O-])=O.[Cs+].[Cs+]>>[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH:13]([F:14])[F:15])[N:6]2[CH:17]([CH3:21])[C:18]([NH2:20])=[O:19]参加物
4
反応条件
- 温度
- 90 °C
実験手順
Synthesized as described in Example 4 using 4-chloro-2-(difluoromethyl)-1H-indole-5-carbonitrile, 2-bromo-propionamide (2 eq) and Cs2CO3 (2 eq). After heating at 90° C. for 4 h, additional 2-bromo-propionamide (2 eq) and Cs2CO3 (2 eq) were added and the reaction mixture heated at 110° C. for 15 h: MS (ES) m/z 298 (M+1).
後処理
- customSynthesized
- temperaturethe reaction mixture heated at 110° C. for 15 h
出典と根拠
- ORDレコード
- ord-a29cdb4e6cd84f11928fc358f443b916
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08673948B2
関連ノート
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