Toluene → HCID 57910772, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 2
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
- customat rt
- temperatureAfter cooling to rt
- filtrationthe reaction mixture was filtered through a short column of CELITE®
- washeluting with EtOAc
- washThe filtrate was washed with water, brine
- dry with materialdried (sodium sulfate)
- concentrationconcentrated in vacuo
- 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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