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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563950Generated: October 26, 2026

Potassium Acetate → 1-{3-[(dipyridin-3-ylamino)methyl]pyridine-2-yl}-3-methyl-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/563950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant1-methyl-2,3-dihydro-1H-1,3-benzodiazol-2-oneHCID 590540—
ReactantN-[(2-chloropyridin-3-yl)methyl]-N-pyridin-3-ylpyridin-3-amineHCID 59138879—
CatalystCopperHCID 23978—
SolventPyridineHCID 1049—
SolventSodium BicarbonateHCID 516892—
Product1-{3-[(dipyridin-3-ylamino)methyl]pyridine-2-yl}-3-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 59138882—

Reaction Steps

To a solution of N-[(2-chloropyridin-3-yl)methyl]-N-pyridin-3-ylpyridin-3-amine (59 mg, 020 mmol) and 1-methyl-2-benzimidazolinone (45 mg, 0.30 mmol) in dry pyridine (1 mL) was added potassium acetate (51 mg, 0.512 mmol), cuprous chloride (11.6 mg, 0.117 mmol), and copper powder (31 mg, 0.487 mmol). This mixture was sealed and heated at 120 C for 4 days. The cooled reaction was diluted with NaHCO3 solution and the product extracted into methylene chloride. This solution was dried over anhydrous sodium sulfate, filtered, and the solvent evaporated This residue was subjected to chromatography on silica gel eluting with a 20-100% acetone/hexane gradient to give the title compound after trituration with diethyl ether as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067607B2
Source datasetuspto-grants-2011_11
ORD IDord-eb8cac8cc76448aeb5351125ce8b130c
Source noteuspto-grants-2011_11