Water → HCID 57687717, compound
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH:14]=[C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:12]=[C:11]2[S:20][C:21]2[CH:26]=[CH:25][C:24]([N+:27]([O-])=O)=[CH:23][CH:22]=2)=[CH:6][CH:5]=1)([O-])=O.[Cl-].[Ca+2].[Cl-].O>C(O)C.[Fe]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH:14]=[C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:12]=[C:11]2[S:20][C:21]2[CH:22]=[CH:23][C:24]([NH2:27])=[CH:25][CH:26]=2)=[CH:6][CH:5]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Ethyl 1-(4-nitrophenyl)-2-[(4-nitrophenyl)thio]-1H-imidazole-4-carboxylate (3.00 g) was suspended in ethanol (120 mL), iron powder (4.05 g), anhydrous calcium chloride (0.81 g) and water (20 mL) were added, and the mixture was heated under reflux for 4 hr. The reaction mixture was allowed to cool, and filtered. Saturated aqueous sodium hydrogen carbonate solution was added to the obtained filtrate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Methanol (30 mL) was added to the residue and the resulting crystals were collected by filtration to give the title compound as pale-yellow crystals (yield 2.00 g, 78%).
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for 4 hr
- temperatureto cool
- filtrationfiltered
- additionSaturated aqueous sodium hydrogen carbonate solution was added to the obtained filtrate
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- additionMethanol (30 mL) was added to the residue
- filtrationthe resulting crystals were collected by filtration
Sources & evidence
- ORD record
- ord-0eebd4cc083341ac8f1f6e9fe6aa05ed
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686010B2
Reaction notes
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