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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368400Generated: October 30, 2026

N-methyl-2-pyrrolidone → 2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)pyridine

https://huagongshe.com/reaction/368400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-MethoxybenzylamineHCID 75452—
Reactant3,5,6-Trifluoropyridin-2-amineHCID 12508074—
SolventChloroformHCID 6212—
Product2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)pyridineHCID 2212125664.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

To 10 ml of N-methylpyrrolidone were added 3.90 g of 2-amino-3,5,6-trifluoropyridine and 7.60 g of p-methoxybenzylamine, and the mixture was stirred under nitrogen atmosphere at 140° C. for one day and allowed to cool. To the solution was added 50 ml of chloroform, and the solution was washed three times with 500 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was subjected to chromatography (silica gel, 32 g; eluent: chloroform) to obtain 4.50 g of the title compound as a pale yellow crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133284
Source datasetuspto-grants-2000_10
ORD IDord-63d921abb72d410f952ae7750a5fbeb8
Source noteuspto-grants-2000_10