戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 466562作成日:2026年10月26日

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

https://huagongshe.com/reaction/466562

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-(m-Tolyl)piperazineHCID 83111—
反応物3-Chloro-6-(methylsulfonyl)pyridazineHCID 252476—
溶媒BenzeneHCID 241—
生成物3-[4-(3-Methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazineHCID 1512460189%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157035
出典データセットuspto-grants-1992_10
ORD IDord-4747d6ab4c074086be6054a49c67d4fd
出典メモuspto-grants-1992_10