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HRID 4292生成日期:2026年10月23日

2,3-二氨基吡啶 → 2-Amino-3-(2-methylbenzylamino)pyridine

https://huagongshe.com/zh-CN/reaction/4292

反应方程式

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)pyridineHCID 1382589134.4%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US04725601
来源数据集uspto-grants-1988_02
ORD IDord-8afe18d01bb54bda9ec3d89b8bd7890e
来源说明uspto-grants-1988_02