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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181030Generated: November 3, 2026

Methanol → Methyl 2-methyl-3h-imidazo[4,5-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/2181030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant5-bromo-2-methyl-3H-imidazo[4,5-b]pyridineHCID 22387961—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
ProductMethyl 2-methyl-3h-imidazo[4,5-b]pyridine-5-carboxylateHCID 22387777—

Reaction Steps

Palladium acetate (1.18 g), 1,3-bis(diphenylphosphino)-propane (2.31 g) and 5-bromo-2-methyl-1H-imidazo[4,5-b]pyridine (3.72 g) were charged in an autoclave, and N,N-dimethylformamide (18.6 ml), methanol (14.9 ml) and triethylamine (5.4 ml) were added. The mixture was stirred at 85° C. for 14 hr in a 10 atm. carbon monoxide atmosphere. The reaction mixture was allowed to cool and the solvent was evaporated. Methanol (60 ml) was added to the residue and heated, and the insoluble matter was filtered off while hot. The filtrate was concentrated to give methyl 2-methyl-1H-imidazo[4,5-b]pyridine-5-carboxylate (2.95 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890934B2
Source datasetuspto-grants-2005_05
ORD IDord-458bf0479bd8479298a7a9579ddaf1af
Source noteuspto-grants-2005_05