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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1657407생성일: 2026년 10월 27일

1-(m-Tolyl)piperazine → 2-Methyl-3-[2-(4-m-tolyl-1-piperazinyl)ethyl]-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/1657407

반응식

참여 물질

역할이름HCID투입량
반응물1-(m-Tolyl)piperazineHCID 83111—
반응물2-methyl-3-(2-chloroethyl)-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 12414940—
용매TolueneHCID 1140—
생성물2-Methyl-3-[2-(4-m-tolyl-1-piperazinyl)ethyl]-7-chloro-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 1241485339.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03960863
출처 데이터셋uspto-grants-1976_06
ORD IDord-b2a14c58a0274586a01eddf82c134411
출처 메모uspto-grants-1976_06