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 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | 4-(Piperazin-1-yl)benzonitrile | HCID 2733995 | — |
| 溶媒 | Hexamethylphosphoramide | HCID 12679 | — |
| 生成物 | 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedione | HCID 20272865 | 29.9% |
反応手順
A mixture of 20.5 g (0.10 mole) of 5-bromo-6-methyl-2,4(1H,3H)-pyrimidinedione, 18.1 g (0.10 mole) of 4-(4-cyanophenyl)piperazine, 6.4 g (0.11 mole) of anhydrous potassium fluoride, 15.2 g (0.1 mole) of powdered potassium carbonate in 100 ml of hexamethyl phosphoramide was heated at 140° C. for 24 hours. The mixture was cooled and poured into 500 ml of ice water. The solid was collected and washed with 100 ml of water. Recrystallization from N,N-dimethylformamide and drying in vacuo at 78° C. for 16 hours gave 9.3 g of the product as a dull solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04532240 |
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| 出典データセット | uspto-grants-1985_07 |
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| ORD ID | ord-5fd490a8d73246e0a4b4afa32a29c68a |
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| 出典メモ | uspto-grants-1985_07 |
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