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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371454생성일: 2026년 10월 27일

1-Benzylpiperazine → 6-Methyl-5-[4-(phenylmethyl)-1-piperazinyl]-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/371454

반응식

참여 물질

역할이름HCID투입량
반응물1-BenzylpiperazineHCID 75994—
반응물2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl-HCID 84757—
반응물Potassium fluoride dihydrateHCID 23708904—
생성물6-Methyl-5-[4-(phenylmethyl)-1-piperazinyl]-2,4(1H,3H)-pyrimidinedioneHCID 13478329—

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 130 ml of 1-benzylpiperazine was heated under reflux for 72 hours. The reaction mixture was then cooled and poured into 800 ml of ice water. The solid which formed was collected and washed with water to give 8.10 g of the product as an off-white solid. A 1.0 g portion of the crude product was recrystallized from methanol to give an off-white solid, mp 263° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532240
출처 데이터셋uspto-grants-1985_07
ORD IDord-b268680494234b9691676094c3fcf777
출처 메모uspto-grants-1985_07