HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 4-(3-chlorophenyl)-6-methyl-N-(3-phenyl-2-propen-1-yl)-2-(pyridine-3-yl)-5-pyrimidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propene-1-yl)acrylamide | HCID 54139120 | — |
| Reactant | HCID 178479320 | HCID 178479320 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-chlorophenyl)-6-methyl-N-(3-phenyl-2-propen-1-yl)-2-(pyridine-3-yl)-5-pyrimidinecarboxamide | HCID 69072866 | — |
Reaction Steps
100 mg (0.294 mmol) of 2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamide was dissolved in 5 ml of DMF. 60.1 mg (0.381 mmol) of 3-amidinopyridinium hydrochloride and 28.9 mg of (0.353 mmol) of sodium acetate were added thereto and stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate and washed with saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The obtained residue was stirred at 120° C. overnight, cooled down at room temperature and purified by the silica gel chromatography (hexane/ethyl acetate=1/2) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07494989B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-90a0c4668b2146dba25dd2fcc36b7208 |
| Source note | uspto-grants-2009_02 |