HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Sodium 3-Benzoyl-5-(4,6-dimethoxypyrimidin-2-yl)oxy-2-trifluoromethylbenzofuran-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | 3-Benzoyl-5-hydroxy-2-trifluoromethylbenzofuran-4-carboxylic acid | HCID 19077271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Sodium 3-Benzoyl-5-(4,6-dimethoxypyrimidin-2-yl)oxy-2-trifluoromethylbenzofuran-4-carboxylate | HCID 23681721 | 40.5% |
Reaction Steps
While stirring 0.35 g of sodium hydride in 30 ml of N,N-dimethylformamide at room temperature, 1.73 g of 3-benzoyl-5-hydroxy-2-trifluoromethylbenzofuran-4-carboxylic acid was gradually added thereto. After completion of the addition, the mixture was further stirred for one hour. While stirring this mixture at room temperature, 1.08 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine was added thereto, and then the mixture was stirred at 70° C. for 3 hours. The mixture was returned to room temperature and poured into water. Precipitated crystals were separated by filtration and washed with water and acetone to obtain 1.02 g (yield: 40.5%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616537 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-a516fc01f4ed45c7a2381437f5b9547c |
| Source note | uspto-grants-1997_04 |