Sodium hydride → HCID 23079305, compound
Reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=[O:7].I[CH2:9][CH2:10][O:11][CH2:12][O:13][CH3:14].[H-].[Na+]>CN(C=O)C>[CH3:14][O:13][CH2:12][O:11][CH2:10][CH2:9][N:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=[O:7]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In DMF (15 ml), 2-imidazole carboxaldehyde (300 mg) was dissolved. Then, the compound (1.01 g) obtained in Example 92-1 and sodium hydride (137 mg) were added to the solution, and the whole was stirred at room temperature for 5 days. After completion of the reaction, the solvent was distilled off and the residue was then added with chloroform, followed by washing with water and saturated saline solution. The resultant was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was purified through silica gel column chromatography (chloroform/methanol), thereby obtaining the subject compound (457 mg) as a yellow viscous liquid.
Workup
- customAfter completion of the reaction
- distillationthe solvent was distilled off
- additionthe residue was then added with chloroform
- washby washing with water and saturated saline solution
- dry with materialThe resultant was dried with anhydrous sodium sulfate
- distillationthe solvent was distilled off
- customSubsequently, the residue was purified through silica gel column chromatography (chloroform/methanol)
Sources & evidence
- ORD record
- ord-273fab7831ab4aab9145fdf5b9e7e3a4
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176227B2
Reaction notes
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