反応式
Br[C:2]1[C:8]([F:9])=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[F:10].C(=O)([O-])[O-].[Cs+].[Cs+].[CH:17]1([B-](F)(F)F)[CH2:19][CH2:18]1.[K]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.I.C12(P(C34CC5CC(CC(C5)C3)C4)CCCC)CC3CC(CC(C3)C1)C2.O.C1(C)C=CC=CC=1>[CH:17]1([C:2]2[C:8]([F:9])=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=2[F:10])[CH2:19][CH2:18]1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 100 °C
実験手順
To a pressure tube was added 4-bromo-3,5-difluoroaniline (1.0 g, 4.8 mmol), cesium carbonate (4.7 g, 14.4 mmol), toluene (10 mL) and water (1 mL). The solution was de-gassed with N2 gas for 30 minutes, followed by the addition of cyclopropyltrifluoro-borate, potassium salt (0.8 g, 5.3 mmol), di(1-adamantyl)-n-butylphosphine hydroiodide (0.07 g, 0.14 mmol) and palladium(II) acetate (0.02 g, 0.096 mmol). De-gassing was continued for 5 minutes, the tube was sealed and heated at 100° C. for 18 hours. The cooled solution was diluted with EtOAc, washed with H2O and brine, dried (Na2SO4), and filtered. The filtrate was treated with 3-mercaptopropyl silica gel for 1 hour. The mixture was filtered and concentrated to give crude product which was purified by flash chromatography (0-30% EtOAc/hexane) to give the title compound (0.67 g, 4.0 mmol, 82%).
後処理
- customThe solution was de-gassed with N2 gas for 30 minutes
- customDe-gassing
- customthe tube was sealed
- additionThe cooled solution was diluted with EtOAc
- washwashed with H2O and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- additionThe filtrate was treated with 3-mercaptopropyl silica gel for 1 hour
- filtrationThe mixture was filtered
- concentrationconcentrated
- customto give crude product which
- customwas purified by flash chromatography (0-30% EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-9e4d9da843e449fe9bdd8ae3aa784ffa
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08921514B2
関連ノート
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