Cesium carbonate → 4-Cyclopropyl-3,5-difluoroaniline

HRID 1411413

反応式

HRID 1411413 の反応式
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

9

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

  1. customThe solution was de-gassed with N2 gas for 30 minutes
  2. customDe-gassing
  3. customthe tube was sealed
  4. additionThe cooled solution was diluted with EtOAc
  5. washwashed with H2O and brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. additionThe filtrate was treated with 3-mercaptopropyl silica gel for 1 hour
  9. filtrationThe mixture was filtered
  10. concentrationconcentrated
  11. customto give crude product which
  12. 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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