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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4292Generated: October 23, 2026

2,3-Diaminopyridine → 2-Amino-3-(2-methylbenzylamino)pyridine

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Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DiaminopyridineHCID 9956—
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product2-Amino-3-(2-methylbenzylamino)pyridineHCID 1382589134.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725601
Source datasetuspto-grants-1988_02
ORD IDord-8afe18d01bb54bda9ec3d89b8bd7890e
Source noteuspto-grants-1988_02