Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-(m-Tolyl)piperazine → 2-Methyl-3-[2-(4-m-tolyl-1-piperazinyl)ethyl]-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-(m-Tolyl)piperazine | HCID 83111 | — |
| 반응물 | 2-methyl-3-(2-chloroethyl)-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 12414940 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-Methyl-3-[2-(4-m-tolyl-1-piperazinyl)ethyl]-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 12414853 | 39.9% |
반응 단계
A mixture of 1.3 g of 2-methyl-3-(2-chloroethyl)-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-one, 2.1 g of 1-(m-tolyl)piperazine and 20 ml of toluene was refluxed for 30 hours. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The obtained residue was purified by means of column chromatography using alumina and recrystallized from a mixture of ethanol and n-hexane to give 0.8 g of the desired compound as pale yellow scales, m.p. 119° - 120°C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US03960863 |
| 출처 데이터셋 | uspto-grants-1976_06 |
| ORD ID | ord-b2a14c58a0274586a01eddf82c134411 |
| 출처 메모 | uspto-grants-1976_06 |