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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073800Generated: November 2, 2026

Triethylamine → 8-(2-Methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2073800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-6-methoxycarbonylaminobenzyl chlorideHCID 14368480—
Reactant8-Amino-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridineHCID 14499805—
SolventMethanolHCID 887—
Product8-(2-Methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridineHCID 1449982538.8%

Reaction Steps

To a solution of 8-amino-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine (8.0 g) and triethylamine (4.8 g) in methanol (80 ml) was added 2-methyl-6-methoxycarbonylaminobenzyl chloride (10.15 g) and the mixture was stirred at room temperature for 17 hours. After methanol was evaporated in vacuo, the resultant residue was dissolved in methylene chloride (100 ml) and the mixture was washed with water and dried over magnesium sulfate. The solvent was evaporated in vacuo. The resultant residue was subjected to column chromatography on silica gel (240 g) and eluted with a mixture of chloroform and ethyl acetate (20:1) to give a crystalline product. The crystals were recrystallized from a mixture of ethyl acetate and n-hexane to give 8-(2-methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine (6.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920129
Source datasetuspto-grants-1990_04
ORD IDord-667a7a3e21ed4e049018afdfeeeac1ca
Source noteuspto-grants-1990_04