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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035483Generated: November 2, 2026

Aniline → 4-(Benzylamino)-6-(phenylamino)pyridine-3-carboxyamide

https://huagongshe.com/reaction/2035483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMethanesulfonic AcidHCID 6395—
Reactant4-Benzylamino-6-chloropyridine-3-carboxyamideHCID 131730930—
SolventChloroformHCID 6212—
SolventDiphenyl EtherHCID 7583—
Product4-(Benzylamino)-6-(phenylamino)pyridine-3-carboxyamideHCID 13173093299.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

To 25 mg of 4-(benzylamino)-6-chloropyridine-3-carboxyamide suspended in 0.2 mL of diphenylether, 18 mg of aniline and 9 mg of methanesulfonic acid were added and stirred at 180° C. for 30 minutes. After cooling, the reaction mixture was dissolved in chloroform, washed with saturated aqueous sodium bicarbonate, and dried on anhydrous sodium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (chloroform:methanol=40:1-10:1) to obtain 30 mg (99%) of the title compound as a slight yellow crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575153B2
Source datasetuspto-grants-2013_11
ORD IDord-6aa3dddddf274305bec1a3c073ea61a8
Source noteuspto-grants-2013_11