反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:13]([C:14]3[CH:19]=[CH:18][C:17]([N+:20]([O-:22])=O)=[CH:16][CH:15]=3)=[CH:12][CH:11]=[N:10]2)=[CH:5][CH:4]=1.[C:23]1([CH3:32])[CH:28]=[CH:27][C:26]([CH2:29]C#N)=[CH:25][CH:24]=1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:13]([C:14]3[CH:19]=[CH:18][C:17]4=[N:20][O:22][C:32]([C:23]5[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][CH:24]=5)=[C:16]4[CH:15]=3)=[CH:12][CH:11]=[N:10]2)=[CH:5][CH:4]=1参加物
3
実験手順
The title compound, light green solid (32 mg, 25%), MS (ISP) m/z=382.3 [(M+H)+], mp 159° C., was prepared in accordance with the general method of example 1 from 1-(4-methoxy-phenyl)-5-(4-nitro-phenyl)-1H-pyrazole (intermediate G) (100 mg, 353 μmol) and commercially available 2-(p-tolyl)-acetonitrile.
出典と根拠
- ORDレコード
- ord-6b395732ddbf4408904a2bacd55df9d4
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09440962B2
関連ノート
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