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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881801Generated: October 31, 2026

Triethylamine → N1-(2-Methoxy-4-methylbenzyl)-n2-(2-(5-methylpyridin-2-yl)ethyl)oxalamide

https://huagongshe.com/reaction/1881801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-(5-Methylpyridin-2-yl)ethan-1-amineHCID 23068295—
Reactant2-Methoxy-4-methylbenzenemethanamineHCID 58607466—
SolventAcetonitrileHCID 6342—
ProductN1-(2-Methoxy-4-methylbenzyl)-n2-(2-(5-methylpyridin-2-yl)ethyl)oxalamideHCID 1121001915%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2 g of (2-methoxy-4-methylphenyl)methanamine (from step 3) and Et3N (3.7 mL, 2 eq) in dry CH3CN (45 mL) was cooled to 0° C. under N2 atmosphere and ethyl 2-chloro-2-oxoacetate (1.47 mL, 1 eq) was added dropwise. After the addition was complete, the reaction mixture was stirred at room temperature for 4 hours and 2-(5-methylpyridin-2-yl)ethanamine (2.52 g, 1.4 eq, from step 5) was added. The reaction was heated at reflux for 24 hours. After cooling the solvent was removed under reduced pressure and the residue was dissolved in ethyl acetate and washed successively with water and brine, dried over MgSO4, filtered and evaporated. The residue was chromatographed on silica gel (eluent: 25-35% acetone in hexane) and recrystallized from ethyl acetate/hexane and ethanol/water to give 650 mg of N1-(2-methoxy-4-methylbenzyl)-N2-(2-(5-methylpyridin-2-yl)ethyl)oxalamide (15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318947B2
Source datasetuspto-grants-2012_11
ORD IDord-7bb5f489c56541d4bebb18619327f63e
Source noteuspto-grants-2012_11