Sodium Hydroxide → HCID 178524858, compound
Reaction equation
O[N:2]=[C:3]([C:9]([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=1)=O)[C:4]([O:6]CC)=[O:5].[N+:18]([C:21]1[CH:22]=[C:23]([CH:26]=[CH:27][CH:28]=1)[CH2:24][NH2:25])([O-:20])=[O:19].[OH-].[Na+]>C(O)C>[Cl:17][C:14]1[CH:13]=[CH:12][C:11]([C:9]2[NH:25][C:24]([C:23]3[CH:26]=[CH:27][CH:28]=[C:21]([N+:18]([O-:20])=[O:19])[CH:22]=3)=[N:2][C:3]=2[C:4]([OH:6])=[O:5])=[CH:16][CH:15]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 5-(4-chlorophenyl)-2-(3-nitrophenyl)imidazole-4-carboxylate obtained by reacting and treating ethyl 2-hydroxyimino-3-(4-chlorophenyl)-3-oxopropionate and 3-nitrobenzylamine in the same manner as in Starting Material Synthetic Example 1 is dissolved in ethyl alcohol and 1 M aqueous sodium hydroxide solution is added. The mixture is reacted and treated in the same manner as in Starting Material Synthetic Example 2 to give 5-(4-chlorophenyl)-2-(3-nitrophenyl)imidazole-4-carboxylic acid.
Workup
- customThe mixture is reacted
- additiontreated in the same manner as
Sources & evidence
- ORD record
- ord-ebf9be33989b4777888dfa551e44c5a8
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06288061B1
Reaction notes
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