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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887633Generated: October 30, 2026

4-Methoxybenzylamine → 2-((4-Methoxybenzyl)amino)isonicotinonitrile

https://huagongshe.com/reaction/887633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-4-cyanopyridineHCID 568638—
SolventPyridineHCID 1049—
Product2-((4-Methoxybenzyl)amino)isonicotinonitrileHCID 21961378—

Reaction Steps

To pyridine (500 mL) were added 2-chloroisonicotinonitrile (22.0 g, 159 mmole), para-methoxybenzylamine (25 g, 114% Meq.), and NaHCO3 (30 g). The mixture was heated under reflux overnight. After cooling to RT, the mixture was filtered and the filter cake was rinsed with CH2Cl2. The combined filtrate was concentrated to dryness in vacuum to form a yellow solid. This solid is then recrystallized in EtOAc to give a light yellow crystalline compound and the mother liquor was concentrated and subjected to EtOAc again (repeating three times) to yield the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247430B2
Source datasetuspto-grants-2012_08
ORD IDord-c0107d9b7db142a29d6e52ac62614157
Source noteuspto-grants-2012_08