Hydrochloric Acid → 2-carbethoxy-3-[1-{(2-chlorophenyl)methyl}-2-propylthio-1H-imidazol-5-yl]propanoic acid
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][N:9]1[C:13]([CH2:14][CH:15]([C:21]([O:23]CC)=[O:22])[C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:12][N:11]=[C:10]1[S:26][CH2:27][CH2:28][CH3:29].C(=O)([O-])[O-].[Na+].[Na+].C(O)C.Cl>C(Cl)Cl.O>[C:16]([CH:15]([CH2:14][C:13]1[N:9]([CH2:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Cl:1])[C:10]([S:26][CH2:27][CH2:28][CH3:29])=[N:11][CH:12]=1)[C:21]([OH:23])=[O:22])([O:18][CH2:19][CH3:20])=[O:17]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of diethyl [1-{(2-chlorophenyl)methyl}-2- propylthio-1H-imidazol-5-yl]methylmalonate (0.62 g, 1.41 mmol), sodium carbonate (1.5 g, 14.2 mol), ethanol (10 mL) and water (10 mL) was stirred at 25° C. for 18 hours, then heated for 15 minutes on a steam bath. The mixture was cooled, neutralized with aqueous hydrochloric acid solution, and the product was extracted-into methylene chloride, washed with water, dried and concentrated to 0.425 g of product. Crystallization from ethyl acetate/hexane provided 0.23 g 55%) of 2-carbethoxy-3-[1-{(2-chlorophenyl)methyl}-2- propylthio-1H-imidazol-5-yl]propanoic acid; mp 118°-120° C.
Workup
- temperatureheated for 15 minutes on a steam bath
- temperatureThe mixture was cooled
- washwashed with water
- customdried
- concentrationconcentrated to 0.425 g of product
- customCrystallization from ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-48a1f80c1ad14c4c96cdbd85eba2b214
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05444080
Reaction notes
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