Reaction equation
[C:1]([C:5]1[NH:9][N:8]=[C:7]([C:10]([F:13])([F:12])[F:11])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C1C(=O)N([Cl:21])C(=O)C1>CN(C=O)C>[C:1]([C:5]1[NH:9][N:8]=[C:7]([C:10]([F:12])([F:13])[F:11])[C:6]=1[Cl:21])([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following protocol L, 5-tert-butyl-3-trifluoromethyl-1H-pyrazole was treated with NCS in DMF to yield title compound.
Sources & evidence
- ORD record
- ord-d94096fce6874d8d9b7d02e135387424
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449576B1
Linked notes
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