Hydrochloric Acid → HCID 9870622, compound
Reaction equation
C(CC[O:5][C:6]([C:8]1[CH:13]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([Cl:20])[CH:15]=2)[C:12]([C:21](=[O:38])[NH:22][CH2:23][CH2:24][CH:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[C:11]([CH3:39])[NH:10][C:9]=1[CH3:40])=[O:7])#N.[OH-].[Na+].Cl>CO>[Cl:20][C:16]1[CH:15]=[C:14]([CH:13]2[C:12]([C:21](=[O:38])[NH:22][CH2:23][CH2:24][CH:25]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)=[C:11]([CH3:39])[NH:10][C:9]([CH3:40])=[C:8]2[C:6]([OH:7])=[O:5])[CH:19]=[CH:18][CH:17]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
275 mg (0.500 mmol) of 4-(3-chlorophenyl)-2,6-dimethyl-5-(3,3-diphenylpropylcarbamoyl)-1,4-dihydropyridine-3-carboxylic acid 2-cyanoethyl ester was dissolved in 10 ml of methanol. 1 ml of 1 N aqueous sodium hydroxide solution was added and stirred at room temperature for 7.5 hours. After adding 2 N hydrochloric acid, methanol was evaporated under reduced pressure. Water was added to the residue, and precipitates thus formed were taken by the filtration, then washed with water and hexane/ethyl acetate (3/1) and dried under reduced pressure to obtain the title compound.
Workup
- customwas evaporated under reduced pressure
- additionWater was added to the residue
- customprecipitates thus
- customformed
- filtrationwere taken by the filtration
- washwashed with water and hexane/ethyl acetate (3/1)
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-46d159fea78e457ab78b3f3c0b1671b8
- Source dataset
- uspto-grants-2009_02
- Patent number
- US07494989B2
Reaction notes
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