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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166169Generated: October 26, 2026

Triethylamine → ethyl 8-(2-Ethyl-6-methylbenzylamino)-3-methylimidazo[1,2-a]pyridin-2-carboxylate

https://huagongshe.com/reaction/1166169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 8-amino-3-methylimidazo[1,2-a]pyridine-2-carboxylateHCID 22672637—
Reactant2-Ethyl-6-methylbenzaldehydeHCID 22997469—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Productethyl 8-(2-Ethyl-6-methylbenzylamino)-3-methylimidazo[1,2-a]pyridin-2-carboxylateHCID 229974688.1%

Reaction Steps

To a stirred mixture of ethyl 8-amino-3-methylimidazo[1,2-a]pyridin-2-carboxylate (1.53 g, 7.0 mmol) in methanol (25 ml) were added 2-ethyl-6-methylbenzaldehyde (1.1 g, 7.1 mmol), zinc(II)chloride (1.1 g, 8.0 mmol) in methanol (10 ml) and sodium cyanoborohydride (0.5 g, 8.0 mmol). The reaction mixture was refluxed for 4 h. and then stirred at room temperature for 20 h. Triethylamine (2.5 ml) was added and the mixture was stirred for 30 min. and evaporated under reduced pressure. Purification of the residue by column chromatography twice on silica gel using 1) methylene chloride:methanol (95:5) 2) heptane:isopropyl ether (1:5) as eluent gave 0.2 g (8%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613775B1
Source datasetuspto-grants-2003_09
ORD IDord-80da9f086b924dc391ffbf26a527ba0c
Source noteuspto-grants-2003_09