Ethyl Acetate → HCID 178489922, compound
Reaction equation
C(=O)([O-])[O-].[K+].[K+].C([O:10][CH2:11][CH2:12][CH2:13][CH:14]([C:24]1[NH:28][C:27](/[CH:29]=[CH:30]/[C:31]2[CH:36]=[CH:35][C:34]([N:37]3[CH:41]=[C:40]([CH3:42])[N:39]=[CH:38]3)=[C:33]([O:43][CH3:44])[CH:32]=2)=[N:26][N:25]=1)[C:15]1[CH:20]=[C:19]([F:21])[C:18]([F:22])=[C:17]([F:23])[CH:16]=1)(=O)C.C(OCC)(=O)C>CO.[Cl-].[Na+].O>[CH3:44][O:43][C:33]1[CH:32]=[C:31](/[CH:30]=[CH:29]/[C:27]2[NH:28][C:24]([CH:14]([C:15]3[CH:16]=[C:17]([F:23])[C:18]([F:22])=[C:19]([F:21])[CH:20]=3)[CH2:13][CH2:12][CH2:11][OH:10])=[N:25][N:26]=2)[CH:36]=[CH:35][C:34]=1[N:37]1[CH:41]=[C:40]([CH3:42])[N:39]=[CH:38]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Potassium carbonate (210 mg) was added to a solution of 4-{5-{(E)-2-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]vinyl}-4H-[1,2,4]triazol-3-yl}-4-(3,4,5-trifluorophenyl)butyl acetate (400 mg) in methanol (3 mL), and the reaction solution was stirred at room temperature for three hours. Ethyl acetate and brine were added to the reaction solution, and the organic layer was separated. The resulting organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 325 mg of the title compound. The property values of the compound are as follows.
Workup
- customthe organic layer was separated
- dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-3b8dee50ea0b45b597ac259ee332b3bb
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07973033B2
Reaction notes
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