Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187053Generated: October 31, 2026

Triethylamine → 2-Amino-N-[(4-methoxyphenyl)methyl]-3-pyridinecarboxamide

https://huagongshe.com/reaction/2187053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Aminonicotinic acidHCID 72930—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantDiethyl cyanophosphonateHCID 76257—
SolventDimethylformamideHCID 6228—
Product2-Amino-N-[(4-methoxyphenyl)methyl]-3-pyridinecarboxamideHCID 22449746100%

Reaction Steps

2-Aminonicotinic acid (7.15 g) was suspended in N,N-dimethylformamide (100 ml) and 4-methoxybenzylamine (8.12 ml), diethyl cyanophosphonate (9.92 ml) and triethylamine (8.66 ml) were added sequentially with stirring and cooling on ice. The reaction mixture was stirred at room temperature for 15.5 hours, concentrated under reduced pressure, and extracted with ethyl acetate. The extract was washed with water, dried (Na2SO4) and then the solvent was distilled off under reduced pressure to give the title compound (15.9 g, about 100%). Recrystallization from ethyl acetate-ethyl ether yielded a colorless crystal, melting point 165 to 166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407116B1
Source datasetuspto-grants-2002_06
ORD IDord-b29022018ffe4c4e863ca82c73e47cff
Source noteuspto-grants-2002_06