Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192690Generated: November 2, 2026

Ethyl Acetate → 1-(6-Pyridin-4-ylpyrazin-2-yl)-1H-benzimidazol-6-amine

https://huagongshe.com/reaction/2192690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant1-(6-chloropyrazin-2-yl)-1H-benzimidazol-6-amineHCID 58217094—
CatalystHCID 178418397HCID 178418397—
SolventHCID 22495535HCID 22495535—
Product1-(6-Pyridin-4-ylpyrazin-2-yl)-1H-benzimidazol-6-amineHCID 58217161—

Reaction Steps

Under a nitrogen atmosphere a mixture of 1-(6-chloropyrazin-2-yl)-1H-benzimidazol-6-amine (50 mg, 0.20 mmol), 4-pyridylboronic add (30 mg, 0.24 mmol), tetrakis(triphenylphosphine)palladium(0) (23 mg, 0.02 mmol) in toluene-n-propanol (2 mL, 3:1) was treated with 2M aqueous sodium carbonate solution (0.14 mL, 0.84 mmol). The resulting mixture was stirred vigorously whilst being heated under reflux overnight. Upon cooling, the mixture was diluted with ethyl acetate (10 mL) and washed with H2O (1×10 mL). The aqueous phase was extracted with ethyl acetate (10 mL) and the organic layers combined and washed with 0.5M Na2CO3, brine and then dried (Na2SO4). Removal of solvent fit vacuo then yielded crude product, which was purified by column chromatography using dichloromethane-methanol (98:2-91:9) as eluent to furnish the product (32 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329737B2
Source datasetuspto-grants-2012_12
ORD IDord-b1dacd5d79e947fcb784914733abbeb1
Source noteuspto-grants-2012_12