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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368415Generated: October 31, 2026

N-methyl-2-pyrrolidone → 2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridine

https://huagongshe.com/reaction/368415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-MethoxybenzylamineHCID 75452—
Reactant3,5,6-Trifluoro-4-methylpyridin-2-amineHCID 12508092—
SolventChloroformHCID 6212—
Product2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridineHCID 2212127138.7%

Reaction Conditions

Temperature140 °C

Reaction Steps

To 3 ml of N-methylpyrrolidone were added 1.35 g of 2-amino-3,5,6-trifluoro-4-methylpyridine together with 3.0 g of p-methoxybenzylamine, and the mixture was stirred under nitrogen atmosphere at 140° C. for 18 hours and allowed to cool. After adding 30 ml of chloroform, the mixture was washed three times with 300 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to chromatography (silica gel, 20 g; eluent: chloroform:n-hexane, 1:1, and then, chloroform) to obtain 0.90 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-27aacc9ee6fd40bbb7e45e1520283585
Source noteuspto-grants-2000_10