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Potassium Carbonate → 5-[4-(4-Chlorophenyl)-1-piperazinyl]-6-methyl-2,4-(1H, 3H)-pyrimidinedione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl- | HCID 84757 | — |
| 反応物 | 1-(4-Chlorophenyl)piperazine | HCID 97478 | — |
| 反応物 | Potassium fluoride dihydrate | HCID 23708904 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | 5-[4-(4-Chlorophenyl)-1-piperazinyl]-6-methyl-2,4-(1H, 3H)-pyrimidinedione | HCID 54423445 | 18.9% |
反応手順
A mixture of 20.50 g (0.100 mole) of 5-bromo-6-methyl-2,4(1H, 3H)pyrimidinedione, 26.96 g (0.100 mole of 1-(4-chlorophenyl)-piperazine, 10.35 g (0.110 mole) of potassium fluoride dihydrate and 41.40 g (0.300 mole) of potassium carbonate in 200 ml of dimethylsulfoxide was heated at 80° for 72 hours. The reaction mixture was cooled and poured into 1 l of ice water. The solid was collected, washed with water, and recrystallized from ethanol to give 6.05 g of the product as a dull yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04532240 |
| 出典データセット | uspto-grants-1985_07 |
| ORD ID | ord-cd3a279158e743fc8ca4bfc331dc0ccc |
| 出典メモ | uspto-grants-1985_07 |