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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4292Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/4292

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-DiaminopyridineHCID 9956—
Edukt2-MethylbenzaldehydeHCID 10722—
EduktSodium BicarbonateHCID 516892—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
Produkt2-Amino-3-(2-methylbenzylamino)pyridineHCID 1382589134,4%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725601
Quelldatensatzuspto-grants-1988_02
ORD IDord-8afe18d01bb54bda9ec3d89b8bd7890e
Quellennotizuspto-grants-1988_02