Hydrochloric Acid → HCID 86590787, compound
Reaction equation
[OH-].[Na+].[CH:3]1[C:13]2[CH:12]=[CH:11][C:10]3[CH:14]=[CH:15][CH:16]=[CH:17][C:9]=3[C:8](=[C:18]3[CH2:23][CH2:22][N:21]([CH2:24][CH2:25][CH2:26][O:27][C:28]([C:30]4[CH:31]([C:45]5[CH:50]=[CH:49][CH:48]=[C:47]([Cl:51])[CH:46]=5)[C:32]([C:38]([O:40]CCC#N)=[O:39])=[C:33]([CH3:37])[NH:34][C:35]=4[CH3:36])=[O:29])[CH2:20][CH2:19]3)[C:7]=2[CH:6]=[CH:5][CH:4]=1.Cl>CO>[CH:14]1[C:10]2[CH:11]=[CH:12][C:13]3[CH:3]=[CH:4][CH:5]=[CH:6][C:7]=3[C:8](=[C:18]3[CH2:19][CH2:20][N:21]([CH2:24][CH2:25][CH2:26][O:27][C:28]([C:30]4[CH:31]([C:45]5[CH:50]=[CH:49][CH:48]=[C:47]([Cl:51])[CH:46]=5)[C:32]([C:38]([OH:40])=[O:39])=[C:33]([CH3:37])[NH:34][C:35]=4[CH3:36])=[O:29])[CH2:22][CH2:23]3)[C:9]=2[CH:17]=[CH:16][CH:15]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5 ml of methanol and 0.434 ml of 1 N aqueous sodium hydroxide solution were added to 244 mg (0.36 mmol) of 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-(2-cyanoethyl) ester 5-(3-(4-(5H-dibenzo[a,d] cyclohepten-5-ylidene) piperidine-1-yl )propan-1-yl) ester and stirred at room temperature for 5 hours. After adding 1 N hydrochloric acid, precipitates were taken by the filtration and dried under reduced pressure to obtain the title compound.
Workup
- customprecipitates
- filtrationwere taken by the filtration
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-0f187f22c0404982aa18eddd2d369fa1
- Source dataset
- uspto-grants-2009_02
- Patent number
- US07494989B2
Reaction notes
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