HCID 88880313, compound → HCID 70664579, compound
Reaction equation
BrC1C=CC(N/[N:9]=[CH:10]/[CH:11]=[N:12]/[NH:13][C:14]2[CH:19]=[CH:18][C:17]([Br:20])=[CH:16][C:15]=2[F:21])=C(F)C=1>C1(C)C=CC=CC=1.FC(F)(F)S([O-])(=O)=O.[Cu+2].FC(F)(F)S([O-])(=O)=O>[Br:20][C:17]1[CH:18]=[CH:19][C:14]([N:13]2[N:9]=[CH:10][CH:11]=[N:12]2)=[C:15]([F:21])[CH:16]=1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Copper (II) trifluoromethanesulfonate (218 mg, 0.60 mmol) was added to a slurry of (1E,2E)-ethanedial bis[(4-bromo-2-fluorophenyl)hydrazone](2.61 g, 6.04 mmol) in toluene (25 mL). The reaction was heated to reflux and stirred at this temperature overnight. The reaction was allowed to cool and was filtered through celite, and the filter pad was washed with EtOAc (100 mL). The combined filtrates were washed with 1 N aq HCl (3×100 mL), water (100 mL), and brine (100 mL) and then dried (MgSO4), filtered and concentrated. The crude product was purified via flash chromatography using a Varian SF25-40 g column and an eluent of EtOAc in hexanes (0-50%) to afford the title compound as a yellow solid (1.08 g, 73.9%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.44 (ddd, 1 H) 7.47-7.54 (m, 1 H) 7.76 (t, 1 H) 7.90 (s, 2 H).
Workup
- temperatureThe reaction was heated
- temperatureto reflux
- temperatureto cool
- filtrationwas filtered through celite
- washthe filter pad was washed with EtOAc (100 mL)
- washThe combined filtrates were washed with 1 N aq HCl (3×100 mL), water (100 mL), and brine (100 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customThe crude product was purified via flash chromatography
Sources & evidence
- ORD record
- ord-77f48b4896df4f7c9c3554c804668fa1
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08779148B2
Reaction notes
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