参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 2,2'-二吡啶胺 | HCID 14547 | — |
| 反应物 | 氢化钠 | HCID 24758 | — |
| 反应物 | 2-(氯甲基)-1-甲基-1H-苯并咪唑 | HCID 248044 | — |
| 溶剂 | N,N-二甲基甲酰胺 | HCID 6228 | — |
| 产物 | N-[(6-methylpyridin-2-yl)methyl]-N-pyridin-2-ylpyridin-2-amine | HCID 66628202 | — |
反应步骤
To a flask were added 1.1 g of 2,2′-dipyridylamine and 25 ml of N,N-dimethylformamide. To this mixture were added 0.32 g of 60% sodium hydride in mineral oil in small portions, and after stirring at 10 C for ten minutes, 1.2 g of 2-(chloromethyl)-1-methyl-1H-benzimidazole in 5 ml of N,N-dimethylformamide were added. The reaction mixture was stirred at 22 C for several hours, and then quenched with 40 ml water. The product was extracted with 50 ml ethyl acetate, and then extracted with 30 ml of 1M hydrochloric acid, and basified with 3M sodium hydroxide. Following extraction with 20 ml ethyl acetate, the product was purified by silica gel chromatography using 33% ethyl acetate, 62% hexane, and 5% methanol, resulting in an oil which crystallized on standing. After drying, 0.6 g of a yellow solid remained.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07538931B2 |
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| 来源数据集 | uspto-grants-2009_05 |
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| ORD ID | ord-0eb400d52e6e40a6bf283de3978da2fe |
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| 来源说明 | uspto-grants-2009_05 |
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