Potassium Hydroxide → HCID 178428549, compound
Reaction equation
[CH3:1][C:2]1[NH:3][C:4]([C:22]([F:25])([F:24])[F:23])=[C:5]([C:20]#[N:21])[C@H:6]([C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[NH:15][N:14]=[C:13]3[CH3:19])[C:7]=1[C:8]#[N:9].[OH-].[K+:27]>C1COCC1>[C:8]([C:7]1[C@@H:6]([C:10]2[CH:11]=[C:12]3[C:16](=[CH:17][CH:18]=2)[NH:15][N:14]=[C:13]3[CH3:19])[C:5]([C:20]#[N:21])=[C:4]([C:22]([F:23])([F:25])[F:24])[N-:3][C:2]=1[CH3:1])#[N:9].[K+:27]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 39 mg (0.11 mmol) (4R)-2-methyl-4-(3-methyl-1H-indazol-5-yl)-6-(trifluoromethyl)-1,4-dihydropyridine-3,5-dicarbonitrile (Example 5) in THF (2 ml) under argon atmosphere was added 126 μl (0.12 mmol) 1 N aqueous potassium hydroxide solution, and the mixture was stirred under a weak argon stream for 5 days at room temperature. The resulting precipitate was dried in vacuo to yield 44 mg (100% of th.) of the title compound as a solid.
Workup
- customThe resulting precipitate was dried in vacuo
Sources & evidence
- ORD record
- ord-6df3b0c0a8104d8e85640b425c83055c
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422263B2
Reaction notes
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