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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368238Generated: November 1, 2026

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

https://huagongshe.com/reaction/1368238

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 numberUS06573274B1
Source datasetuspto-grants-2003_06
ORD IDord-8f9af6b96fbd43b0bfee90504e379a47
Source noteuspto-grants-2003_06