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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-methyl- | HCID 84757 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 4-(Piperazin-1-yl)benzonitrile | HCID 2733995 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 생성물 | 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-methyl-2,4-(1H,3H)-pyrimidinedione | HCID 20272865 | 29.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04532240 |
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| 출처 데이터셋 | uspto-grants-1985_07 |
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| ORD ID | ord-5fd490a8d73246e0a4b4afa32a29c68a |
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| 출처 메모 | uspto-grants-1985_07 |
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