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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377477Generated: October 30, 2026

Sodium Iodide → 8-(6-Methyl-2-nitrobenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1377477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant2-(chloromethyl)-1-methyl-3-nitroBenzeneHCID 12204070—
Reactant2,3-Dimethylimidazo[1,2-a]pyridin-8-amineHCID 21873980—
SolventAcetoneHCID 180—
Product8-(6-Methyl-2-nitrobenzylamino)-2,3-dimethylimidazo[1,2-a]pyridineHCID 1538242449.5%

Reaction Steps

Sodium iodide (15.0 g) and sodium carbonate (31.0 g) are added to a solution of 8-amino-2,3-dimethylimidazo[1,2-a]pyridine (14.7 g) and 6-methyl-2-nitrobenzylchloride (18.6 g) in acetone (100 ml) at RT and are heated to reflux for 6 h. After cooling to RT and evaporation of the solvent, the residue is dissolved in a mixture of ethyl acetate (200 ml) and water (200 ml), and the organic phase is separated off. After three further extractions with ethyl acetate (100 ml) the combined organic layers are dried over magnesium sulfate and concentrated to a volume of 80 ml. 12.1 g of the title compound crystallize as a faintly yellow solid. The mother liquor is evaporated and the residue is purified by chromatography on silica gel (toluene/dioxane=6:1 as eluent) to yield additional 14 g of crystalline material. After recrystallization of both fractions from ethyl acetate, 21.5 g (76%) of the title compound of m.p. 160°-162° C. are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665730
Source datasetuspto-grants-1997_09
ORD IDord-8cbea724bf9f43308866fc1c1827829d
Source noteuspto-grants-1997_09