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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371471생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/371471

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl-HCID 84757—
반응물Potassium FluorideHCID 522689—
반응물4-(Piperazin-1-yl)benzonitrileHCID 2733995—
용매HexamethylphosphoramideHCID 12679—
생성물5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedioneHCID 2027286529.9%

반응 조건

온도140 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532240
출처 데이터셋uspto-grants-1985_07
ORD IDord-5fd490a8d73246e0a4b4afa32a29c68a
출처 메모uspto-grants-1985_07