Sodium Hydroxide → 2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1H-benzimidazole-4-carbonitrile
反応式
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([CH3:10])[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:4]([N:17]2[CH2:21][CH2:20][C@H:19]([N:22]([CH3:24])[CH3:23])[CH2:18]2)[C:3]=1[NH:25][C:26](=O)[C:27]([CH3:30])([CH3:29])[CH3:28].[OH-].[Na+]>C(O)(=O)C>[C:27]([C:26]1[NH:25][C:3]2[C:4]([N:17]3[CH2:21][CH2:20][C@H:19]([N:22]([CH3:24])[CH3:23])[CH2:18]3)=[C:5]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:6]([CH3:10])=[C:7]([C:8]#[N:9])[C:2]=2[N:1]=1)([CH3:30])([CH3:29])[CH3:28]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
An acetic acid (5 ml) solution of N-[4-amino-5-cyano-2-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-methylbiphenyl-3-yl]-2,2-dimethylpropionamide (I-270) (300 mg, 0.72 mmol) was heated at 80° C. for 2.5 hours. After cooling, the reaction solution was poured into aqueous sodium hydroxide solution (6.7 M, 15 ml).
後処理
- temperatureAfter cooling
出典と根拠
- ORDレコード
- ord-44cfe75dbc2e4b838f77c05a72d46977
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737166B2
反応ノート
読み込み中…