Sodium Carbonate → HCID 67262031, compound
Reaction equation
[CH2:1]([N:4]1[CH:8]=[CH:7][C:6]([C:9]2[S:10][CH:11]=[CH:12][CH:13]=2)=[N:5]1)[CH2:2][CH3:3].C(N1C(C2SC=CC=2)=CC=N1)CC.[I:27]N1C(=O)CCC1=O.S([O-])([O-])(=O)=S.[Na+].[Na+].C(=O)([O-])[O-].[Na+].[Na+]>CN(C)C=O>[I:27][C:7]1[C:6]([C:9]2[S:10][CH:11]=[CH:12][CH:13]=2)=[N:5][N:4]([CH2:1][CH2:2][CH3:3])[CH:8]=1Participants
Procedure
To a mixture of 1-propyl-3-(2-thienyl)-1H-pyrazole and 1-propyl-5-(2-thienyl)-1H-pyrazole (80:20, 5.0 mmol) in 18 mL dry N,N-dimethylformamide under argon atmosphere was added N-iodosuccinimide (5.2 mmol) in small portions. The reaction mixture was stirred overnight at room temperature. 5% aqueous sodium thiosulfate solution and saturated aqueous sodium carbonate solution were added and the mixture was stirred at room temperature for 1 h, then extracted with ethyl acetate. The combined organic extracts were successively washed with water and brine, dried over MgSO4, filtered and concentrated. The residue was purified by chromatography on silica gel (toluene:ethyl acetate 100:0 to 0:100) to afford 180 mg 4-iodo-1-propyl-3-(2-thienyl)-1H-pyrazole (11% yield).
Workup
- stirringthe mixture was stirred at room temperature for 1 h
- extractionextracted with ethyl acetate
- washThe combined organic extracts were successively washed with water and brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by chromatography on silica gel (toluene:ethyl acetate 100:0 to 0:100)
Sources & evidence
- ORD record
- ord-6321344171ef4d4b9d7e83765db04a73
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08685974B2
Reaction notes
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