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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466562생성일: 2026년 10월 25일

Triethylamine → 3-[4-(3-Methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazine

https://huagongshe.com/reaction/466562

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(m-Tolyl)piperazineHCID 83111—
반응물3-Chloro-6-(methylsulfonyl)pyridazineHCID 252476—
용매BenzeneHCID 241—
생성물3-[4-(3-Methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazineHCID 1512460189%

반응 단계

A mixture of 3.2 parts of 3-chloro-6-(methylsulfonyl)pyridazine, 3 parts of 1-(3-methylphenyl)piperazine, 2 parts of N,N-diethylethanamine and 180 parts of benzene was stirred for 24 hours at reflux. The reaction mixture was evaporated. Water was added to the residue. The precipitated product was filtered off, washed with water and dissolved in trichloromethane. The solution was dried, filtered and evaporated. The residue was crystallized from methanol. The product was filtered off and dried, yielding 5 parts (89%) of 3-[4-(3-methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazine; mp. 201° C. (compound 209).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05157035
출처 데이터셋uspto-grants-1992_10
ORD IDord-4747d6ab4c074086be6054a49c67d4fd
출처 메모uspto-grants-1992_10