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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43718Generated: October 26, 2026

2-Chloropyridine → cis(+/-)-4-Chloro-N-(3-ethoxy-1-pyridin-2-ylpiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamide

https://huagongshe.com/reaction/43718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyridineHCID 7977—
ReactantSodium CarbonateHCID 10340—
Reactantcis(+/-)-4-Chloro-N-(3-ethoxypiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamide hydrochlorideHCID 86648665—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productcis(+/-)-4-Chloro-N-(3-ethoxy-1-pyridin-2-ylpiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamideHCID 866486673.5%

Reaction Steps

cis(±)-4-Chloro-N-(3-ethoxypiperidin-4-yl)-5-ethyl-1H-imidazole-2-carboxamide hydrochloride obtained in Example (131a) (100 mg, 0.297 mmol), 2-chloropyridine (0.035 mL, 0.37 mmol) and sodium carbonate (157 mg, 1.48 mmol) were suspended in DMF (1 mL), and the suspension was heated using a microwave reactor at 180° C. for 30 minutes. The reaction solution was diluted with ethyl acetate, washed with water and brine, and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=7/3→1/0) to obtain 3.9 mg of the title compound as a white amorphous solid (3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-3e4d5f62bcc44bf2a0349bb740c8890d
Source noteuspto-grants-2013_09