参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 2,3-二氨基吡啶 | HCID 9956 | — |
| 反应物 | 2-甲基苯甲醛 | HCID 10722 | — |
| 反应物 | 碳酸氢钠 | HCID 516892 | — |
| 反应物 | 氰基硼氢化钠 | HCID 5003444 | — |
| 溶剂 | 醋酸 | HCID 176 | — |
| 溶剂 | (5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮 | HCID 887 | — |
| 产物 | 2-Amino-3-(2-methylbenzylamino)pyridine | HCID 13825891 | 34.4% |
反应步骤
Molecular Sieves (16 g) was added to a solution of 2,3-diaminopyridine (8 g), 2-methylbenzaldehyde (8.81 g), and acetic acid (4.2 ml) in methanol (160 ml) and the mixture was stirred for 96 hours at room temperature. Sodium cyanoborohydride (4.61 g) was added portionwise to the mixture with stirring under ice-cooling over a period of 20 minutes. After being stirred for 3 hours, the mixture was made alkaline with aqueous sodium bicarbonate solution and filtered by suction. The filtrate was evaporated in vacuo, and to the residue was added water and then extracted with methylene chloride. The extract was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of ethyl acetate and n-hexane to give 2-amino-3-(2-methylbenzylamino)pyridine (5.38 g).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US04725601 |
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| 来源数据集 | uspto-grants-1988_02 |
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| ORD ID | ord-8afe18d01bb54bda9ec3d89b8bd7890e |
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| 来源说明 | uspto-grants-1988_02 |
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