1392274-42-8 → 1586046-21-0
Reaction equation
CN1C(C(F)(F)F)=C([B:11]2[O:15][C:14]([CH3:17])([CH3:16])[C:13]([CH3:19])([CH3:18])[O:12]2)C=N1.Br[C:21]1[C:22]([CH3:28])=[N:23][N:24]([CH3:27])[C:25]=1[F:26]>>[F:26][C:25]1[N:24]([CH3:27])[N:23]=[C:22]([CH3:28])[C:21]=1[B:11]1[O:15][C:14]([CH3:17])([CH3:16])[C:13]([CH3:19])([CH3:18])[O:12]1Participants
3
Procedure
Following the procedure of Intermediate 149, replacing 4-bromo-1-methyl-5-(trifluoromethyl)pyrazole with 4-bromo-5-fluoro-1,3-dimethyl-1H-pyrazole (commercial) provided the title compound.
Sources & evidence
- ORD record
- ord-828668f681ac415f8e36b09192255126
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09328106B2
Reaction notes
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