1,4-Dioxane → HCID 86695924, 화합물

HRID 2369521노트

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HRID 2369521 반응식
Cl[C:2]1[C:7]([C:8]([O-:10])=[O:9])=[CH:6][N:5]=[CH:4][C:3]=1[F:11].[Cl:12][C:13]1[CH:18]=[CH:17][C:16](B(O)O)=[C:15]([F:22])[CH:14]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].O1CCOC[CH2:32]1>O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([C:2]2[C:7]([C:8]([O:10][CH3:32])=[O:9])=[CH:6][N:5]=[CH:4][C:3]=2[F:11])=[C:15]([F:22])[CH:14]=1

참가 물질

7

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온도
80 °C

실험 절차

To a solution of 4-chloro-5-fluoronicotinate (1.2 g, 6.33 mmol) in 1,4-dioxane (12 mL) and water (0.5 mL) was added (4-chloro-2-fluorophenyl)boronic acid (1.214 g, 6.96 mmol) and potassium phosphate, dibasic (2.205 g, 12.66 mmol). To this mixture, PdCl2(dppf) (0.371 g, 0.506 mmol) was added and the solution purged with N2 for 10 min then heated to 80° C. for 12 h. The mixture was cooled to room temperature and water (25 mL) was added. The solution was extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with brine (25 mL) and concentrated under reduced pressure to afford the residue which was purified by silica gel column using a gradient of ethyl acetate in hexanes to afford methyl 4-(4-chloro-2-fluorophenyl)-5-fluoronicotinate (900 mg, 3.17 mmol, 50% yield) as a yellow solid. LCMS (ESI) m/e 284.0 [(M+H)+, calcd for C13H9ClF2NO2 284.0]; LC/MS retention time (Method F): tR=1.01 min.

후처리

  1. customthe solution purged with N2 for 10 min
  2. temperatureThe mixture was cooled to room temperature
  3. additionwater (25 mL) was added
  4. extractionThe solution was extracted with ethyl acetate (3×25 mL)
  5. washThe combined organic layers were washed with brine (25 mL)
  6. concentrationconcentrated under reduced pressure
  7. customto afford the residue which
  8. customwas purified by silica gel column

출처 및 근거

ORD 기록
ord-32a1a72a9d02492fbebc918bc389e83e
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08703953B2

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