反応式
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=2)=[O:8])[NH:4][N:3]=1.O1CCOCC1.Cl[C:24]1[C:33]2[C:28](=[CH:29][C:30]([O:36][CH2:37][CH2:38][CH2:39][Cl:40])=[C:31]([O:34][CH3:35])[CH:32]=2)[N:27]=[CH:26][N:25]=1.ClCCl>CC(N(C)C)=O.Cl>[Cl:40][CH2:39][CH2:38][CH2:37][O:36][C:30]1[CH:29]=[C:28]2[C:33]([C:24]([NH:1][C:2]3[CH:6]=[C:5]([C:7]([NH:9][C:10]4[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=4)=[O:8])[NH:4][N:3]=3)=[N:25][CH:26]=[N:27]2)=[CH:32][C:31]=1[O:34][CH3:35]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
3-Amino-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamide (153 mg, 0.69 mmol) in dimethylacetamide (1.8 ml) and HCl in dioxane (4 M solution in dioxane, 174 μl, 0.69 mmol) was reacted with 4-chloro-7-(3-chloropropoxy)-6-methoxyquinazoline (200 mg, 0.69 mmol) at 90° C. for 1.5 hour. Dichloromethane (35 ml) was added to the cooled reaction mixture, and the solid recovered by filtration, washed with dichloromethane and dried to yield 3-{[7-(3-chloropropoxy)-6-methoxyquinazolin-4-yl]amino}-N-(3-fluorophenyl)-1H-pyrazole-5-carboxamide (286 mg, 81% yield):
後処理
- filtrationthe solid recovered by filtration
- washwashed with dichloromethane
- customdried
出典と根拠
- ORDレコード
- ord-4dc25890c54c435fb884c5cabd4bf5ab
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07402585B2
関連ノート
読み込み中…