Hydrochloric Acid → HCID 21090872, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:13]([C:14]3[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[CH:16][CH:15]=3)=[CH:12][C:11]([C:22]([F:25])([F:24])[F:23])=[N:10]2)=[CH:5][CH:4]=1.[ClH:26]>CO.[Pd]>[ClH:26].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[C:13]([C:14]3[CH:21]=[CH:20][C:17]([CH2:18][NH2:19])=[CH:16][CH:15]=3)=[CH:12][C:11]([C:22]([F:25])([F:23])[F:24])=[N:10]2)=[CH:7][CH:8]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 4-[1-(4-methoxyphenyl)-3-(trifluoro-methyl)-1H-pyrazol-5-yl]benzonitrile obtained by Example 56 (430 mg), Pd/C (100 mg) and 1N hydrochloric acid (1.3 ml) in methanol (43 ml) was stirred under Hydrogen atmosphere for 5 hrs.
Sources & evidence
- ORD record
- ord-a48b3f0be1f148d0a47ab3bd77d046d7
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183306B2
Reaction notes
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