Sodium Hydroxide → 4-(2-Chloro-6-fluorophenyl)-3-cyclopentyloxycarbonyl-1,4-dihydro-2,6-dimethylpyridine-5-carboxylic acid
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH:9]1[C:14]([C:15]([O:17][CH:18]2[CH2:22][CH2:21][CH2:20][CH2:19]2)=[O:16])=[C:13]([CH3:23])[NH:12][C:11]([CH3:24])=[C:10]1[C:25]([O:27]CCC#N)=[O:26].[OH-].[Na+]>COCCOC>[CH:18]1([O:17][C:15]([C:14]2[CH:9]([C:3]3[C:4]([F:8])=[CH:5][CH:6]=[CH:7][C:2]=3[Cl:1])[C:10]([C:25]([OH:27])=[O:26])=[C:11]([CH3:24])[NH:12][C:13]=2[CH3:23])=[O:16])[CH2:19][CH2:20][CH2:21][CH2:22]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
98 g (0.22 mol) of 2-cyanoethyl cyclopentyl 4-(2-chloro-6-fluorophenyl)-1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate are dissolved in 400 ml of 1,2-dimethoxyethane and the solution is stirred with 400 ml of 1 N sodium hydroxide solution at room temperature overnight.
Sources & evidence
- ORD record
- ord-16aee0a088c845a18f69588b96182922
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06066655
Reaction notes
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