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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579965Generated: October 25, 2026

Ethylamine → 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/579965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantNitroethaneHCID 6587—
ReactantImidazo[1,2-a]pyridine-6-carbaldehydeHCID 7164582—
CatalystButylamineHCID 8007—
SolventEthanolHCID 702—
Product6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridineHCID 5391556811.9%

Reaction Steps

In 40 ml of ethanol, 6.9 g of 6-imidazo[1,2-a]-pyridinecarbaldehyde was stirred under reflux for 14 hours, together with 10.6 g of nitroethane and 30 drops of n-butyl amine. Then, a small quantity of ethyl amine was added thereto and the mixture was stirred under reflux for further 18 hours. After insoluble matter was removed by filtration upon heating, 50 ml of ethanol and 150 ml of ether were further added to remove insoluble matter by filtration. The solvent was removed by distillation under reduced pressure and the residue was recrystallized twice from ethanol to obtain 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751227
Source datasetuspto-grants-1988_06
ORD IDord-8b9f5d263fd647a7b2d1a3d7cd77fe6c
Source noteuspto-grants-1988_06