Water → N-(3-cyano-2,4-difluorophenyl)-N,1-dimethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide
Reaction equation
[C:1](=O)([O-])[O-].[K+].[K+].IC.[C:9]([C:11]1[C:12]([F:38])=[C:13]([NH:18][C:19]([C:21]2[N:25]([CH3:26])[N:24]=[C:23]([C:27]([F:33])([F:32])[C:28]([F:31])([F:30])[F:29])[C:22]=2[C:34]([F:37])([F:36])[F:35])=[O:20])[CH:14]=[CH:15][C:16]=1[F:17])#[N:10].O>CN(C=O)C>[C:9]([C:11]1[C:12]([F:38])=[C:13]([N:18]([CH3:1])[C:19]([C:21]2[N:25]([CH3:26])[N:24]=[C:23]([C:27]([F:32])([F:33])[C:28]([F:31])([F:30])[F:29])[C:22]=2[C:34]([F:36])([F:37])[F:35])=[O:20])[CH:14]=[CH:15][C:16]=1[F:17])#[N:10]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Potassium carbonate (1.28 g, 5.58 mmol, 2.0 eq.) and iodomethane (0.5 ml, 1.2 g, 8.4 mmol, 3.0 eq.) were added to a solution of N-(3-cyano-2,4-difluorophenyl)-1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide (1.25 g, 2.79 mmol) in DMF (4 ml). After 5 h, water was added, the mixture was extracted with ethyl acetate and the extract was washed with sat. aq. sodium chloride solution and dried over MgSO4. Filtration through silica gel gave N-(3-cyano-2,4-difluorophenyl)-N,1-dimethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide (1.27 g, 98%) as a mixture of rotamers which was reacted further without additional purification.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washthe extract was washed with sat. aq. sodium chloride solution
- dry with materialdried over MgSO4
- filtrationFiltration through silica gel
Sources & evidence
- ORD record
- ord-8c1b14c2b18546a8b0e399acc3b5075a
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09204645B2
Reaction notes
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