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)piperazine | HCID 71252181 | 15.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US08816079B2 |
|---|
| 来源数据集 | uspto-grants-2014_08 |
|---|
| ORD ID | ord-eb0674f3edd244f3995b85e2b604a5a1 |
|---|
| 来源说明 | uspto-grants-2014_08 |
|---|