Potassium Carbonate → HCID 68842349, compound
Reaction equation
[F:1][C:2]([F:9])([F:8])[C:3]1[CH:7]=[CH:6][NH:5][N:4]=1.[CH2:10]([O:17][C:18]1[CH:23]=[C:22]([CH2:24]Br)[CH:21]=[CH:20][C:19]=1[N+:26]([O-:28])=[O:27])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH2:10]([O:17][C:18]1[CH:23]=[C:22]([CH:21]=[CH:20][C:19]=1[N+:26]([O-:28])=[O:27])[CH2:24][N:5]1[CH:6]=[CH:7][C:3]([C:2]([F:9])([F:8])[F:1])=[N:4]1)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-trifluoromethyl-1H-pyrazole (632 mg, 4.65 mmol) and 2-benzyloxy-4-bromomethyl-1-nitrobenzene (1.0 g, 3.1 mmol) in DMF (8 mL) is added K2CO3 (642 mg, 4.65 mmol) and the mixture is stirred at RT for 48 h. The mixture is partitioned between EtOAc and water and the organic phase is washed with brine and dried over MgSO4. The solvent is removed under reduced pressure to give the title compound: (M+1)+=378.
Workup
- customThe mixture is partitioned between EtOAc and water
- washthe organic phase is washed with brine
- dry with materialdried over MgSO4
- customThe solvent is removed under reduced pressure
Sources & evidence
- ORD record
- ord-ffd8378248104d13945381d994f72e1d
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084448B2
Reaction notes
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