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HRID 2411226生成日期:2026年10月23日

N,N-二异丙基乙胺 → 1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine

https://huagongshe.com/zh-CN/reaction/2411226

反应方程式

参与物

角色名称HCID投料
反应物N,N-二异丙基乙胺HCID 81531—
反应物N,N-双-2-氯乙基对甲苯磺酸胺HCID 96039—
反应物2,4-二甲基-5-氨基吡啶HCID 7060669—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
产物1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazineHCID 7125218115.7%

反应步骤

To 5-amino-2,4-dimethylpyridine (883 mg) were added N,N-diisopropylethylamine (2.1 mL) and N,N-bis(2-chloroethyl)-p-toluenesulfonamide (2.08 g), and the mixture was stirred with heating under reflux. After completion of the reaction, water was added to the reaction mixture, the mixture was extracted with chloroform, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg). The obtained 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg) was dissolved in acetic acid (2 mL), 40% hydrobromic acid (2 mL) was added, and the mixture was stirred at 100° C. After completion of the reaction, the reaction mixture was neutralized with aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer to give the title compound (131 mg).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08816079B2
来源数据集uspto-grants-2014_08
ORD IDord-eb0674f3edd244f3995b85e2b604a5a1
来源说明uspto-grants-2014_08