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HRID 371471作成日:2026年10月26日

Potassium Carbonate → 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/371471

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl-HCID 84757—
反応物Potassium FluorideHCID 522689—
反応物4-(Piperazin-1-yl)benzonitrileHCID 2733995—
溶媒HexamethylphosphoramideHCID 12679—
生成物5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedioneHCID 2027286529.9%

反応条件

温度140 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04532240
出典データセットuspto-grants-1985_07
ORD IDord-5fd490a8d73246e0a4b4afa32a29c68a
出典メモuspto-grants-1985_07