Sodium Hydroxide → HCID 67133057, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:7]([CH:28]2[CH2:30][CH2:29]2)[C:8]([C:17]2[CH:22]=[CH:21][C:20]([O:23][C:24]([F:27])([F:26])[F:25])=[CH:19][CH:18]=2)=[N:9][C:10]=1[C:11]1[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=1)=[O:5])C.[OH-].[Na+:32]>CCO>[Na+:32].[CH:28]1([N:7]2[C:6]([C:4]([O-:5])=[O:3])=[C:10]([C:11]3[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=3)[N:9]=[C:8]2[C:17]2[CH:22]=[CH:21][C:20]([O:23][C:24]([F:26])([F:27])[F:25])=[CH:19][CH:18]=2)[CH2:30][CH2:29]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 0.9 g (2 mmol) 3-cyclopropyl-5-pyridin-3-yl-2-(4-trifluoromethoxy-phenyl)-3H-imidazole-4-carboxylic acid ethyl ester in 5 ml of EtOH was added 0.4 ml of 6 M sodium hydroxide solution (2 mmol) and the mixture heated to reflux for 6 h. The solvent was then evaporated, affording 1.0 g (quant.) of the title compound as a white solid. MS: 390.1 (MH+).
Workup
- temperaturethe mixture heated
- temperatureto reflux for 6 h
- customThe solvent was then evaporated
Sources & evidence
- ORD record
- ord-dfd3d56ac12c41eabb9493bd99049aa9
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07935707B2
Reaction notes
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