Toluene → HCID 57910772, compound

HRID 1968675Notes

Reaction equation

HRID 1968675 reaction equation
[CH3:1][C:2]([C:21]1[CH:26]=[CH:25][C:24]([C:27]2[N:28]=[N:29][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:31][CH:32]=2)=[CH:23][CH:22]=1)([C:6]1[CH:11]=[CH:10][C:9](B2OC(C)(C)C(C)(C)O2)=[CH:8][N:7]=1)[CH:3]([CH3:5])[CH3:4].Br[C:38]1[CH:39]=[N:40][CH:41]=[C:42]([O:44][CH3:45])[CH:43]=1.C(=O)([O-])[O-].[Na+].[Na+].C1(C)C=CC=CC=1>CCO.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]>[CH3:1][C:2]([C:6]1[N:7]=[CH:8][C:9]([C:38]2[CH:39]=[N:40][CH:41]=[C:42]([O:44][CH3:45])[CH:43]=2)=[CH:10][CH:11]=1)([C:21]1[CH:22]=[CH:23][C:24]([C:27]2[N:28]=[N:29][C:30]([C:33]([F:34])([F:35])[F:36])=[CH:31][CH:32]=2)=[CH:25][CH:26]=1)[CH:3]([CH3:4])[CH3:5]

Participants

7

Conditions

Temperature
95 °C

Procedure

[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (14.0 mg, 0.0190 mmol) was added to a stirred solution of 8d (47.0 mg, 0.0950 mmol), 3-bromo-5-methoxypyridine (23.0 mg, 4.43 mmol) and sodium carbonate (100 μL of a 2.0 M aqueous solution, 0.200 mmol) in EtOH:toluene (500 μL of an 80:20 mixture, respectively) at rt. The resulting solution was heated to 95° C. for approximately 5 h. After cooling to rt, the reaction mixture was filtered through a short column of CELITE®, eluting with EtOAc. The filtrate was washed with water, brine, dried (sodium sulfate) and concentrated in vacuo. The crude residue was purified by flash chromatography on silica gel (gradient elution; 20%-50% EtOAc/hexanes as eluent) to furnish the title compound 8e. m/z (ES) 479 (MH)+.

Workup

  1. customat rt
  2. temperatureAfter cooling to rt
  3. filtrationthe reaction mixture was filtered through a short column of CELITE®
  4. washeluting with EtOAc
  5. washThe filtrate was washed with water, brine
  6. dry with materialdried (sodium sulfate)
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was purified by flash chromatography on silica gel (gradient elution; 20%-50% EtOAc/hexanes as eluent)

Sources & evidence

ORD record
ord-d4262918631d4d8280ea5d765f6bc1d4
Source dataset
uspto-grants-2013_04
Patent number
US08426413B2

Reaction notes

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