HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4292Generated: October 23, 2026
2,3-Diaminopyridine → 2-Amino-3-(2-methylbenzylamino)pyridine
https://huagongshe.com/en/reaction/4292
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Reactant | 2-Methylbenzaldehyde | HCID 10722 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-3-(2-methylbenzylamino)pyridine | HCID 13825891 | 34.4% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04725601 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-8afe18d01bb54bda9ec3d89b8bd7890e |
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| Source note | uspto-grants-1988_02 |
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