HCID 66995417, compound → HCID 136368380, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([C:18]2[CH:19]=[C:20]([CH:25]=[CH:26][N:27]=2)[C:21]([O:23][CH3:24])=[O:22])[CH:6]=[C:7]([F:17])[C:8]=1[O:9]CC1C=CC=CC=1)#[N:2]>CO.C1COCC1.[C].[Pd]>[C:1]([C:3]1[CH:4]=[C:5]([C:18]2[CH:19]=[C:20]([CH:25]=[CH:26][N:27]=2)[C:21]([O:23][CH3:24])=[O:22])[CH:6]=[C:7]([F:17])[C:8]=1[OH:9])#[N:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Methyl 2-(3-cyano-4-benzyloxy-5-fluorophenyl)isonicotinate is stirred at room temperature in methanol-THF (1:1) under a hydrogen atmosphere at normal pressure in the presence of palladium-carbon to obtain methyl 2-(3-cyano-5-fluoro-4-hydroxyphenyl)isonicotinate. FN: 271.
Sources & evidence
- ORD record
- ord-adb2b66cc0e149a3b40867dfeb81b3e8
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07820700B2
Reaction notes
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