참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chloropyridine hydrochloride | HCID 81852 | — |
| 반응물 | Piperazin-2-one | HCID 231360 | — |
| 생성물 | 4-(Pyridin-4-YL)piperazin-2-one | HCID 18918356 | 23.5% |
반응 단계
An intimate mixture of piperazinone (4.2 g) and 4-chloropyridine hydrochloride (7.33 g) was stirred and heated at 200° C. for 10 minutes and allowed to cool. The product was purified by flash column chromatography and cluted with 1/9/0.1 v:v:v methanol/methylene chloride/0.88 S.G. aqueous ammonia. The solid thus obtained was recrystallised from ethanol to give 4-(4-pyridyl)piperazin-2-one (1.75 g); m.p. 268°-270° C.; NMR (d6DMSO) δ 8.2(3H,m); 6.8(12H,m); 3.85(2H,s); 3.52(2H,m); 3.31(2H,m); m/e 178(M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05750754 |
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| 출처 데이터셋 | uspto-grants-1998_05 |
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| ORD ID | ord-e94f1e26e68d489da0de721b108a7220 |
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| 출처 메모 | uspto-grants-1998_05 |
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