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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371472생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/371472

반응식

참여 물질

역할이름HCID투입량
반응물1-PhenylpiperazineHCID 7096—
반응물2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl-HCID 84757—
반응물Potassium fluoride dihydrateHCID 23708904—
생성물6-Methyl-5-(4-phenyl-1-piperazinyl)-2,4(1H, 3H)-pyrimidinedione, hydrateHCID 131714289—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532240
출처 데이터셋uspto-grants-1985_07
ORD IDord-8ef45b1fe7da4a5ab02088c7701be9d0
출처 메모uspto-grants-1985_07