反応式
[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:14][CH2:13][C@@H:12]([N:15]([CH3:24])[C:16]3[CH:23]=[CH:22][C:19]([C:20]#[N:21])=[CH:18][N:17]=3)[CH2:11]2)=[N:3][CH:2]=1.[Cl-].N.[N-:27]=[N+:28]=[N-:29].[Na+]>CN(C)C=O>[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:14][CH2:13][C@@H:12]([N:15]([CH3:24])[C:16]3[CH:23]=[CH:22][C:19]([C:20]4[N:27]=[N:28][NH:29][N:21]=4)=[CH:18][N:17]=3)[CH2:11]2)=[N:3][CH:2]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 120 °C
実験手順
A mixture of (R)-6-((1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)(methyl)amino)nicotinonitrile (100 mg, 0.3 mmol), ammonia chloride (84 mg, 1.57 mmol) and sodium azide (108 mg, 1.66 mmol) in N,N-dimethylformamide (5.0 mL) was stirred at 120° C. for 16 h. The volatile was removed under vacuum and the residue was purified by chromatography on silica gel to give the title compound. MS (m/z): 363.0 (M+H)+.
後処理
- customThe volatile was removed under vacuum
- customthe residue was purified by chromatography on silica gel
出典と根拠
- ORDレコード
- ord-ba07618c7dca45be825a729a72254b9b
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09346810B2
関連ノート
読み込み中…