反応式
[F:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][C:3]=1[F:11].C(N(CC)CC)C.Br[CH2:20][C:21]([NH:23][C:24]1[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:33])([F:32])[F:31])[CH:25]=1)=[O:22]>C1(C)C=CC=CC=1.C(OCC)(=O)C>[F:11][C:3]1[CH:4]=[CH:5][C:6]2[N:7]=[CH:8][N:9]([CH2:20][C:21]([NH:23][C:24]3[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:31])([F:32])[F:33])[CH:25]=3)=[O:22])[C:10]=2[C:2]=1[F:1]参加物
実験手順
To a suspension of 4,5-difluoro-1H-benzimidazole (20 mg, 0.13 mmol) in toluene (260 μL), triethylamine (18 μL, 0.13 mmol) and 2-bromo-N-[3-(trifluoromethyl)phenyl]acetamide (37 mg, 0.13 mmol) were added. The reaction mixture was microwave-irradiated in a sealed vial at 120° C. for 30 min. The vial was cooled, opened and the contents dissolved in 20 mL ethyl acetate. The solution was washed with water (5 mL), saturated aqueous NaHCO3 (5 mL) and brine (5 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. Separation of the isomers in the crude product was performed on flash silica column using neat ethyl acetate to yield the title compound (11.3 mg, 25%). MS (ESI) m/z: 355.8 [M+H] 1H NMR (400 MHz, MeOD) δ ppm 5.31 (s, 2H), 7.20 (ddd, J=11.4, 9.0, 7.5 Hz, 1H), 7.40 (d, J=7.8 Hz, 1H), 7.47 (ddd, J=8.9, 3.7, 1.3 Hz, 1H), 7.52 (t, J=8.1 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.96 (s, 1H), 8.20 (s, 1H).
後処理
- additionwere added
- customThe reaction mixture was microwave-irradiated in a sealed vial at 120° C. for 30 min
- temperatureThe vial was cooled
- washThe solution was washed with water (5 mL), saturated aqueous NaHCO3 (5 mL) and brine (5 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated under reduced pressure
- customSeparation of the isomers in the crude product
出典と根拠
- ORDレコード
- ord-09f8c0b82a214a57862cb7729af5df37
- 出典データセット
- uspto-grants-2010_01
- 特許番号
- US07645784B2
関連ノート
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