反応式
[NH2:1][C:2]1[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=1)=O.[CH:17]1([C:20](=O)[CH2:21][C:22]([O:24][CH3:25])=[O:23])[CH2:19][CH2:18]1.S(=O)(=O)(O)O>CO>[CH:17]1([C:20]2[C:21]([C:22]([O:24][CH3:25])=[O:23])=[C:4]([C:6]3[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=3)[C:3]3[C:2](=[CH:16][CH:15]=[CH:14][CH:13]=3)[N:1]=2)[CH2:19][CH2:18]1参加物
反応条件
- 温度
- 25 °C
実験手順
To the solution of 2-amino-4′-fluorobenzophenone (100 g) in methanol (500 ml) added Methyl 3-cyclopropyl-3-oxopropanoate (132 g), sulfuric acid (5 ml) and stirred for 15 minutes at 25° C. Heated the reaction mixture to 65° C. for 22 hrs. Distilled off the methanol completely under reduced pressure. Cooled the reaction mixture to 25° C., added water (500 ml) and stirred for 30 minutes. Cooled the reaction mixture to 0° C. and pH adjusted to 6.0 with sodium carbonate solution. Stirred the reaction mixture for 45 minutes at 25° C. Filtered the cake and washed with water. Spin dry the compound for 60 minutes. To this compound added methanol (150 ml) and stirred for 1 hr at 25° C. Filtered the solid and washed with methanol (50 ml). Dried the obtained solid to get the title compound.
後処理
- temperatureHeated the reaction mixture to 65° C. for 22 hrs
- distillationDistilled off the methanol completely under reduced pressure
- temperatureCooled the reaction mixture to 25° C.
- additionadded water (500 ml)
- stirringstirred for 30 minutes
- temperatureCooled the reaction mixture to 0° C.
- stirringStirred the reaction mixture for 45 minutes at 25° C
- filtrationFiltered the cake
- washwashed with water
- customSpin dry the compound for 60 minutes
- additionTo this compound added methanol (150 ml)
- stirringstirred for 1 hr at 25° C
- filtrationFiltered the solid
- washwashed with methanol (50 ml)
- customDried the obtained solid
出典と根拠
- ORDレコード
- ord-f512dc7c2628429c9c19daab70177297
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08487105B2
関連ノート
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