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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616209Generated: November 1, 2026

Dimethylformamide → 5-chloro-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/1616209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant6-Chloro-N2-methylpyridine-2,3-diamineHCID 24903942—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product5-chloro-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 55269061—

Reaction Conditions

Temperature80 °C

Reaction Steps

6-chloro-N2-methylpyridine-2,3-diamine (1-2) (35 g, 222 mmol) and 1,1′-Carbonyldiimidazole (63 g, 389 mmol) were added to a round bottom flask and suspended in DMF (150 mL). The solution was heated to 80° C. in an oil bath overnight. The reaction was then suspended in ethyl acetate and sodium bicarbonate. The suspension was washed with sodium bicarbonate, brine (×5), dried over sodium sulfate, filtered, and concentrated to produce the solid 5-chloro-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (1-3). MS (M+H)+: observed=184.2, calculated=184.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765784B2
Source datasetuspto-grants-2014_07
ORD IDord-db6485ff96754e5b9cd4b8cecdc71ebc
Source noteuspto-grants-2014_07