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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709633Generated: November 1, 2026

4-Aminopyridine → HCID 14819972, compound

https://huagongshe.com/reaction/1709633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantN-(2-Aminophenyl)-N-(4-methylphenyl)amine hydrochlorideHCID 2331656—
ReactantHCID 14819970HCID 14819970—
SolventChloroformHCID 6212—
ProductHCID 14819972HCID 14819972—

Reaction Steps

2-Chloro-N-[2-[(4-methylphenyl)amino]phenyl]acetamide which had been synthesized from N-(4-methylphenyl)-1,2-benzenediamine by substantially the same manner as described in Reference Example 1 and 4-aminopyridine were dissolved in chloroform and the solution was left on standing under stirring at room temperature overnight, whereby the reaction was completed. The resulting precipitates were collected by filtration and recrystallized from ethanol to give N-[2-[(4-methylphenyl)amino]phenyl]-2-[(4-pyridinyl)amino]-acetamide hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950667
Source datasetuspto-grants-1990_08
ORD IDord-d7aecc1840894ac48135a4e1696aa87f
Source noteuspto-grants-1990_08