Triethylamine → HCID 11233557、化合物

HRID 1991209

反応式

HRID 1991209 の反応式
[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

6

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

  1. additionwere added
  2. customThe reaction mixture was microwave-irradiated in a sealed vial at 120° C. for 30 min
  3. temperatureThe vial was cooled
  4. washThe solution was washed with water (5 mL), saturated aqueous NaHCO3 (5 mL) and brine (5 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. 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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