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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368255Generated: October 30, 2026

Pyridine → HCID 22485177, compound

https://huagongshe.com/reaction/1368255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22485098HCID 22485098—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22485177HCID 22485177—

Reaction Steps

To a mixture of methyl 3-(2-chloro-4-(methylamino)benzyl)-2-methyl-3H-imidazo[4,5-b]pyridine-5-carboxylate dihydrochloride (418 mg), pyridine (396 mg) and tetrahydrofuran (4.2 ml) was added dropwise ethyl chlorocarbonate (0.115 ml) under ice-cooling and the mixture was stirred at room temperature for 6 hr. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated to dryness under reduced pressure. The residue was pulverized in diethyl ether to give methyl 3-(2-chloro-4-(N-ethoxycarbonyl-N-methylamino)benzyl)-2-methyl-3H-imidazo[4,5-b]pyridine-5-carboxylate (340 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573274B1
Source datasetuspto-grants-2003_06
ORD IDord-0f173fba13c643b58047ae6fd560b8f5
Source noteuspto-grants-2003_06