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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406895Generated: October 31, 2026

2-Hydroxy benzimidazole → HCID 66650118, compound

https://huagongshe.com/reaction/2406895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy benzimidazoleHCID 11985—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
ReactantHCID 66650112HCID 66650112—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 66650118HCID 6665011817.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

5-Iodo-4′-methyl-biphenyl-3-carboxylic acid ((S)-1-pyrazin-2-yl-ethyl)-amide (110 mg, 0.25 mmol) was dissolved in toluene (3 mL) and 1,3-dihydro-benzoimidazol-2-one (135 mg, 1.0 mmol), and CuI (15 mg), K3PO4 (212 mg, 1.0 mmol) and 1,2-bis(methylamino)cyclohexane (0.1 mL) were added. The reaction mixture was stirred at 110° C. overnight, then cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was separated and concentrated under reduced pressure and the residue was purified by preparative thin layer chromatography (7% methanol in dichloromethane) to give 20 mg (185 yield overall) of 4′-methyl-5-(2-oxo-2,3-dihydro-benzoimidazol-1-yl)-biphenyl-3-carboxylic acid ((S)-1-pyrazin-2-yl-ethyl)-amide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809402B2
Source datasetuspto-grants-2014_08
ORD IDord-9191200bd0904c22abeca84de6129249
Source noteuspto-grants-2014_08