反応式
[F:1][C:2]1[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10](B2OC(C)(C)C(C)(C)O2)=[CH:9][CH:8]=1)=[O:5].[CH3:27][O:28][C:29](=[O:38])[C:30]1[CH:35]=[CH:34][C:33]([CH3:36])=[C:32](Br)[CH:31]=1.C([O-])([O-])=O.[K+].[K+]>CN1CCCC1=O>[CH3:27][O:28][C:29]([C:30]1[CH:31]=[C:32]([C:10]2[CH:9]=[CH:8][C:7]([NH:6][C:4](=[O:5])[C:3]3[C:22]([F:26])=[CH:23][CH:24]=[CH:25][C:2]=3[F:1])=[CH:12][CH:11]=2)[C:33]([CH3:36])=[CH:34][CH:35]=1)=[O:38]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 suspension of 2,6-difluoro-N-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-benzamide (359 mg, 1 mmol), 3-bromo-4-methyl-benzoic acid methyl ester (228 mg, 1 mmol), benzyl(chloro)bis(triphenylphosphine)palladium (38 mg, 0.05 mmol) and K2CO3 (690 mg, 5 mmol) in 1-methylpyrrolidinone (NMP) (5 ml) was degassed with vacuum and heated at 120° C. for 10 hr. After cooling down to room temperature, ethyl acetate (EtOAc) (200 ml) was added and the mixture was washed with water (60 ml×3). The EtOAc was evaporated and the residue was purified by column chromatography on silica gel (Hexanes:EtOAc) to give Compound 1 (286 mg, yield 75%).
後処理
- customwas degassed with vacuum
- temperatureAfter cooling down to room temperature
- additionethyl acetate (EtOAc) (200 ml) was added
- washthe mixture was washed with water (60 ml×3)
- customThe EtOAc was evaporated
- customthe residue was purified by column chromatography on silica gel (Hexanes:EtOAc)
出典と根拠
- ORDレコード
- ord-8afd4206935246eb92863eb593fc3d1b
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08592486B2
関連ノート
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