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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487970Generated: October 31, 2026

Ethanol → Methyl 4-cyclopropyl-5-(3H-imidazo[4,5-c]pyridin-2-yl)-2-methylbenzoate

https://huagongshe.com/reaction/1487970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3,4-DiaminopyridineHCID 5918—
ReactantMethyl 4-cyclopropyl-5-formyl-2-methylbenzoateHCID 90021238—
SolventSodium BicarbonateHCID 516892—
ProductMethyl 4-cyclopropyl-5-(3H-imidazo[4,5-c]pyridin-2-yl)-2-methylbenzoateHCID 9002175138.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 100-mL round-bottom flask was placed a mixture of methyl 4-cyclopropyl-5-formyl-2-methylbenzoate (compound 87.1, 500 mg, 2.29 mmol), pyridine-3,4-diamine (500 mg, 4.58 mmol), NH4OAc (1.42 g, 18.4 mmol) and ethanol (50 mL). The resulting mixture was stirred open to the air for 3 days at 70° C., then cooled to room temperature and diluted with aqueous sodium bicarbonate (sat., 50 mL). The aqueous phase was extracted with ethyl acetate (2×50 mL) and the combined organic layers were dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate as the eluent to yield 268 mg (38%) of the title compound as a yellow semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-0f440eda1935477abfbf00d5a05b26d0
Source noteuspto-grants-2016_08