Acetone → HCID 86760568, compound
Reaction equation
C[C:2](C)=[O:3].[Cl:5][C:6]1[CH:7]=[C:8]([CH:12]2[C:17]([C:18](=[O:35])[NH:19][CH2:20][CH2:21][CH:22]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[C:16]([CH3:36])[NH:15][C:14]([CH3:37])=[C:13]2C(O)=O)[CH:9]=[CH:10][CH:11]=1.[N+]([O-])([O-])=[O:42].[NH4+].[Ce]>O>[Cl:5][C:6]1[CH:7]=[C:8]([C:12]2[C:17]([C:18](=[O:35])[NH:19][CH2:20][CH2:21][CH:22]([C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[C:16]([CH3:36])[NH:15][C:14]([CH3:37])([C:2]([OH:3])=[O:42])[CH:13]=2)[CH:9]=[CH:10][CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2 ml of acetone was added to 57.3 mg (0.110 mmol) of 4-(3-chlorophenyl)-2,6-dimethyl-5-(3,3-diphenylpropylcarbamoyl)-1,4-dihydropyridine-3-carboxylic acid. 178 mg (0.320 mmol) of cerium ammonium nitrate suspended in 1 ml of water was added and stirred at room temperature for 2.5 hours. After adding water and extracting with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain the title compound.
Workup
- additionwas added
- extractionextracting with ethyl acetate
- dry with materialthe organic layer was dried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-b93316479fae43b2be7da8ceb7b1f91e
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07288544B2
Reaction notes
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