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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686130Generated: November 3, 2026

Triethylamine → HCID 67265766, compound

https://huagongshe.com/reaction/1686130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-(5-Methylpyridin-2-yl)ethan-1-amineHCID 23068295—
ReactantHCID 67265413HCID 67265413—
SolventAcetonitrileHCID 6342—
ProductHCID 67265766HCID 6726576630%

Reaction Steps

To a mixture of 1.8 g of (2-methoxy-4-methylphenyl)methanamine hydrochloride salt and triethylamine (5.1 mL, 3 equiv.) in dry acetonitrile (45 mL) was added ethyl 2-chloro-2-oxoacetate (1.47 mL, 1 equiv.) dropwise at 0° C. under nitrogen atmosphere. After the addition was complete, the reaction mixture was stirred at room temperature for 2 hours and 2-(5-methylpyridin-2-yl)ethanamine (2.52 g, 1.4 equiv.) was added. The reaction was heated at reflux for 24 hours. After removal of the solvent, the residue was dissolved in ethyl acetate and washed successively with water and brine, dried over MgSO4, filtered, and evaporated. The residue was washed with methyl t-butyl ether (20 mL) and recrystallized from ethanol to give 1.3 g of N′-(2-methoxy-4-methylbenzyl)-N2-(2-(5-methylpyridin-2-yl)ethyl) oxalamide as a white powder (yield 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148536B2
Source datasetuspto-grants-2012_04
ORD IDord-4fca418732464d858780166cb78e8d94
Source noteuspto-grants-2012_04