Cesium carbonate → HCID 66652860, 화합물

HRID 509110노트

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HRID 509110 반응식
[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

참가 물질

6

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온도
80 °C

실험 절차

[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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-383024d36c16475783a4e6292c32564a
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09096558B2

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