Cesium carbonate → HCID 66652860、化合物

HRID 509110

反応式

HRID 509110 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1B(O)O.C(=O)([O-])[O-].[Cs+].[Cs+].Br.Br[C:23]1[CH:28]=[CH:27][N:26]=[N:25][CH:24]=1>O1CCOCC1.O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1[C:23]1[CH:28]=[CH:27][N:26]=[N:25][CH:24]=1

参加物

6

反応条件

温度
80 °C

実験手順

[2-Chloro-5-(trifluoromethyl)phenyl]boronic acid (0.410 g, 1.83 mmol), caesium carbonate (1.1 g, 3.38 mmol) and 4-bromopyridazine hydrobromide (Preparation 20, 0.35 g, 1.46 mmol) were dissolved in 1,4-dioxane (3.5 mL) and water (1 mL). The mixture was heated to 80° C. under nitrogen then palladium tetrakis triphenylphosphine (0.085 g, 0.074 mmol) was added. The reaction was stirred for three hours before it was left to cool to room temperature. The mixture was subsequently filtered through Arbocel®, then diluted in ethyl acetate (15 mL) and washed twice with a saturated solution of aqueous brine (15 mL). The organic layer was collected, dried over sodium sulphate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (ISCO™, 0-50% ethyl acetate in heptane gradient elution, 12 g SiO2) to give title compound as a green solid (0.23 g, 61%).

後処理

  1. waitwas left
  2. temperatureto cool to room temperature
  3. filtrationThe mixture was subsequently filtered through Arbocel®
  4. additiondiluted in ethyl acetate (15 mL)
  5. washwashed twice with a saturated solution of aqueous brine (15 mL)
  6. customThe organic layer was collected
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by silica gel column chromatography (ISCO™, 0-50% ethyl acetate in heptane gradient elution, 12 g SiO2)

出典と根拠

ORDレコード
ord-383024d36c16475783a4e6292c32564a
出典データセット
uspto-grants-2015_08
特許番号
US09096558B2

関連ノート

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