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【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.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 11292 3,6-Dichloropyridazine 141-30-0 C4H2Cl2N2 详情 详情
(II) 11293 1-(3-Methylphenyl)piperazine 41186-03-2 C11H16N2 详情 详情
(III) 11294 3-Chloro-6-[4-(3-methylphenyl)piperazino]pyridazine C15H17ClN4 详情 详情
Extended Information