5-Methyl-2-(1-methyl-1H-pyrazol-4-yl)benzoic acid → 5-Methyl-2-(1-methyl-1H-pyrazol-3-yl)benzoic acid
Reaction equation
CC1C=CC(C2C=NN(C)C=2)=C(C=1)C(O)=O.[CH3:17][C:18]1[CH:19]=[CH:20][C:21]([C:28]2[CH:32]=[CH:31][N:30]([CH3:33])[N:29]=2)=[C:22]([CH:27]=1)[C:23]([O:25]C)=[O:24]>>[CH3:17][C:18]1[CH:19]=[CH:20][C:21]([C:28]2[CH:32]=[CH:31][N:30]([CH3:33])[N:29]=2)=[C:22]([CH:27]=1)[C:23]([OH:25])=[O:24]Participants
3
Procedure
The title compound was synthesized following the same general protocol as described for 5-methyl-2-(1-methyl-1H-pyrazol-4-yl)benzoic acid in Example A1, using methyl 5-methyl-2-(1-methyl-1H-pyrazol-3-yl)benzoate. ESI-MS (m/z): 217 [M+1]+.
Sources & evidence
- ORD record
- ord-67855b517a70445c9dbc560a4f6e1e32
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440982B2
Reaction notes
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