戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 371472作成日:2026年10月26日

1-Phenylpiperazine → 6-Methyl-5-(4-phenyl-1-piperazinyl)-2,4(1H, 3H)-pyrimidinedione, hydrate

https://huagongshe.com/reaction/371472

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenylpiperazineHCID 7096—
反応物2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl-HCID 84757—
反応物Potassium fluoride dihydrateHCID 23708904—
生成物6-Methyl-5-(4-phenyl-1-piperazinyl)-2,4(1H, 3H)-pyrimidinedione, hydrateHCID 131714289—

反応手順

A mixture of 20.5 g (0.10 mole) of 5-bromo-6-methyl-2,4(1H, 3H)-pyrimidinedione and 10.3 g (0.11 mole) of potassium fluoride dihydrate in 150 ml of 1-phenylpiperazine was heated under reflux at 105° for 72 hours and cooled. The reaction mixture was poured into 200 ml of ice water. The solid was collected, washed with water, and recrystallized from methanol to give 7.12 g of the product as a white solid, mp>300° C.

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-8ef45b1fe7da4a5ab02088c7701be9d0
出典メモuspto-grants-1985_07