Ethyl Acetate → HCID 24852339, compound
Reaction equation
[H-].[Na+].Cl[CH2:4][CH2:5][NH:6][C:7]([C:9]1[N:10]=[C:11](/[CH:21]=[CH:22]/[C:23]2[CH:28]=[CH:27][C:26]([N:29]3[CH:33]=[C:32]([CH3:34])[N:31]=[CH:30]3)=[C:25]([O:35][CH3:36])[CH:24]=2)[NH:12][C:13]=1[C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)=[O:8].C(OCC)(=O)C.O.C(=O)(O)[O-].[Na+]>CN(C=O)C>[F:20][C:17]1[CH:18]=[CH:19][C:14]([C:13]2[N:12]=[C:11](/[CH:21]=[CH:22]/[C:23]3[CH:28]=[CH:27][C:26]([N:29]4[CH:33]=[C:32]([CH3:34])[N:31]=[CH:30]4)=[C:25]([O:35][CH3:36])[CH:24]=3)[N:10]3[CH2:4][CH2:5][NH:6][C:7](=[O:8])[C:9]=23)=[CH:15][CH:16]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (containing mineral oil at 60%, 3 mg) was added to a solution of 5-(4-fluorophenyl)-2-{(E)-2-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]vinyl}-1H-imidazole-4-carboxylic acid (2-chloroethyl)amide (15 mg) in DMF (2 mL) at room temperature, and the reaction solution was stirred at room temperature for 30 minutes. Ethyl acetate and saturated sodium bicarbonate water were added to the reaction solution, and the organic layer was separated. The resulting organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: ethyl acetate->ethyl acetate:methanol=5:1) to obtain 10 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
- customThe residue was purified by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: ethyl acetate->ethyl acetate:methanol=5:1)
Sources & evidence
- ORD record
- ord-f804ca5569354f97aa1faa8e6a736c8a
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07713993B2
Reaction notes
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