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【结 构 式】

【分子编号】57015

【品名】3-chloro-6-(1-piperazinyl)pyridazine

【CA登记号】

【 分 子 式 】C8H11ClN4

【 分 子 量 】198.655

【元素组成】C 48.37% H 5.58% Cl 17.85% N 28.2%

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)

The condensation of 3,6-dichloropyridazine (I) with piperazine (II) by means of TEA in refluxing toluene gives 3-chloro-6-(1-piperazinyl)pyridazine (III), which is methylated with HCHO/ HCOOH at 110 C, yielding 3-chloro-6-(4-methylpiperazin-1-yl)pyridazine (IV). Finally, this compound is quaternized with methyl iodide in ethyl ether to provide the target dimethylpiperidinium salt.

1 Toma, L.; et al.; 6-Chloropyridazin-3-yl derivatives active as nicotinic agents: Synthesis, binding, and modeling studies. J Med Chem 2002, 45, 18, 4011.
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) 10355 Diethylenediamine; Piperazine 110-85-0 C4H10N2 详情 详情
(III) 57015 3-chloro-6-(1-piperazinyl)pyridazine C8H11ClN4 详情 详情
(IV) 53381 3-chloro-6-(4-methyl-1-piperazinyl)pyridazine 27464-17-1 C9H13ClN4 详情 详情
Extended Information