【结 构 式】 |
【分子编号】11294 【品名】3-Chloro-6-[4-(3-methylphenyl)piperazino]pyridazine 【CA登记号】 |
【 分 子 式 】C15H17ClN4 【 分 子 量 】288.77964 【元素组成】C 62.39% H 5.93% Cl 12.28% N 19.4% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(III)N-Alkylation of 1-(3-methylphenyl)piperazine with 3,6-dichloropyridazine in dimethylformamide as a solvent and in the presence of sodium carbonate afforded 3-chloro-6-[4-(3-methylphenyl-1-piperazinyl]pyridazine. The reactive chlorine atom in this intermediate was replaced by a methoxy group, by refluxing the compound in methanol containing an excess of sodium methoxide. After addition of water to the cooled reaction mixture the product crystallized. Recrystallization from 2-propanol produced pure 3-methoxy-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine.
【1】 Andries, K.; Stokbroekx, R.; R 61837. Drugs Fut 1990, 15, 3, 237. |
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