3-(4-Cyano-1H-pyrazol-5-yl)-4-methylbenzoic acid → HCID 178425893, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[N:5][NH:6][C:7]=1[C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[CH3:17])[C:11]([OH:13])=[O:12])#[N:2].I[C:19]1NN=C(C)C=1C#N.IC1C(C#N)=CNN=1>>[C:1]([C:3]1[C:4]([CH3:19])=[N:5][NH:6][C:7]=1[C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][C:16]=1[CH3:17])[C:11]([OH:13])=[O:12])#[N:2]Participants
4
Procedure
The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 256.5, except 5-iodo-3-methyl-1H-pyrazole-4-carbonitrile (compound 257.4) was used in place 3-iodo-1H-pyrazole-4-carbonitrile (compound 256.1).
Sources & evidence
- ORD record
- ord-4f6539a277264608b42b67d427a49a6b
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428502B2
Reaction notes
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