Cesium carbonate → 4-Iodo-1-(2,2,2-trifluoroethyl)-1H-pyrazole
Reaction equation
[I:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[F:13][C:14]([F:18])([F:17])[CH2:15]I>CN(C=O)C>[I:1][C:2]1[CH:3]=[N:4][N:5]([CH2:15][C:14]([F:18])([F:17])[F:13])[CH:6]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
In a microwave vial 4-iodo-1H-pyrazole (1.00 g, 5.16 mmol) and cesium carbonate (6.72 g, 20.6 mmol) were suspended in DMF (8.0 mL) and 1,1,1-trifluoro-2-iodoethane (2.06 mL, 20.6 mmol) was added. The mixture was heated at 90° C. by microwave for 60 minutes then the mixture was filtered and the filter cake rinsed with EtOAc. The filtrate was concentrated then taken up in EtOAc and 50% saturated aqueous NH4Cl. The organic layer was washed with sat LiCl and sat NaCl then dried over MgSO4. The solution was concentrated and the residue purified by SiO2 chromatography (5-35% EtOAc/heptane) to afford 1.08 g (76%) of 4-iodo-1-(2,2,2-trifluoroethyl)-1H-pyrazole as a colorless oil.
Workup
- filtrationthe mixture was filtered
- washthe filter cake rinsed with EtOAc
- concentrationThe filtrate was concentrated
- washThe organic layer was washed with sat LiCl
- dry with materialthen dried over MgSO4
- concentrationThe solution was concentrated
- customthe residue purified by SiO2 chromatography (5-35% EtOAc/heptane)
Sources & evidence
- ORD record
- ord-21b55ddfe1e34d57815bf7a2f0642532
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08518945B2
Reaction notes
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