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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35520Generated: October 26, 2026

2-Amino-5-methylpyridine → 6-Methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/35520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylpyridineHCID 15348—
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product6-Methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridineHCID 749917—

Reaction Steps

59.5 g (0.2 mole) of 1-bromo-2-(4-nitrophenyl)-2-ethanone, 21.6 g (0.2 mole) of 2-amino-5-methylpyridine and 34 g of sodium bicarbonate are reacted in 200 ml of 95% strength ethanol. Stirring and refluxing are maintained for 3 hours, and the reaction mixture is then cooled and the ethanol evaporated off under reduced pressure. The evaporation residue is stirred in 700 ml of water at 70° C. for 3 hours, and the insoluble material is then filtered off, washed with 50 ml of ethanol and then ether and dried. M.p. 237°-239° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767755
Source datasetuspto-grants-1988_08
ORD IDord-0a808d8832164fd696ba306bfcf7bb18
Source noteuspto-grants-1988_08