反応式
Cl.[NH2:2][C:3]1[CH:4]=[C:5]([CH:21]=[CH:22][CH:23]=1)[CH2:6][NH:7][C:8]1[C:17]2[C:12](=[C:13]([C:18]([NH2:20])=[O:19])[CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][N:9]=1.Cl[C:25]1[C:30]2[N:31]=[CH:32][N:33]([CH3:34])[C:29]=2[CH:28]=[CH:27][N:26]=1>>[CH3:34][N:33]1[C:29]2[CH:28]=[CH:27][N:26]=[C:25]([NH:2][C:3]3[CH:4]=[C:5]([CH:21]=[CH:22][CH:23]=3)[CH2:6][NH:7][C:8]3[C:17]4[C:12](=[C:13]([C:18]([NH2:20])=[O:19])[CH:14]=[CH:15][CH:16]=4)[N:11]=[CH:10][N:9]=3)[C:30]=2[N:31]=[CH:32]1参加物
3
実験手順
The title compound was prepared according to Example 549 starting 4-(3-Amino-benzylamino)-quinazoline-8-carboxylic acid amide hydrochloride and 4-Chloro-1-methyl-1H-imidazo[4,5-c]pyridine. Reaction conditions: 120° C. in the microwave for 10 h:
後処理
- customReaction conditions
出典と根拠
- ORDレコード
- ord-f1d50868dcbe421c874179990e7b0e91
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637532B2
関連ノート
読み込み中…