Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | HCID 19910246 | HCID 19910246 | — |
| Product | HCID 15070268 | HCID 15070268 | — |
Reaction Steps
4.5 g of ethyl 2-hydroxy-3-methyl-3-phenylbutyric acid, 4,6 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine, 5,3 g of anhydrous potassium carbonate and 50 ml of N,N-dimethylformamide were introduced to a round bottom flask, and the mixture was stirred at 100° C. for 3 hours. Then, the reaction mixture was poured into ice water and extracted twice with 50 ml of ethyl acetate. The extract was washed with water and then dried over anhydrous sodium sulfate overnight. An inorganic salt was removed by filtration, and then the solvent was distilled off under reduced pressure to obtain 7 g of crude crystals. The crude crystals were recrystallized from ethanol to obtain 5.6 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05087289 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-98aec370201447f8a8c464f163f7c93d |
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| Source note | uspto-grants-1992_02 |
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