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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189253Generated: October 30, 2026

2-Iodopyridine → 7-chloro-1-methyl-2-(4-(pyridin-2-yl)but-3-ynyl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/1189253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodopyridineHCID 221126—
Reactant2-(but-3-ynyl)-7-chloro-1-methyl-1H-benzo[d]imidazoleHCID 86086884—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product7-chloro-1-methyl-2-(4-(pyridin-2-yl)but-3-ynyl)-1H-benzo[d]imidazoleHCID 665980106%

Reaction Steps

In a dry reaction tube containing copper iodide (1 mg, 0.0055 mmol) and triethylamine (0.50 mL, 0.1 mmol), were added 2-iodopyridine (22 mg, 0.11 mmol) and Pd(PPh3)2Cl2 (2.4 mg, 0.0055 mmol). A yellow suspension was obtained and after a few minutes of stirring at room temperature, 2-(but-3-ynyl)-7-chloro-1-methyl-1H-benzo[d]imidazole (compound 191(E), 24 mg, 0.11 mmol) in triethylamine (0.2 mL) was added. Immediately the color of the reaction turns to black. The mixture was stirred at room temperature for 30 min and then at 50° C. for 3 h. Triethylamine was concentrated under reduce pressure and the residue was dissolved in DCM. The organic layer was washed with saturated NH4Cl, water and brine. The solvent was removed under reduced pressure and the crude product was purified by flash chromatography system (prepacked silicagel column 2 g, DCM/MeOH:98/2 as eluent) to afford 2 mg g of 7-chloro-1-methyl-2-(4-(pyridin-2-yl)but-3-ynyl)-1H-benzo[d]imidazole (Yield: 6%) as brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-22b08f25833a44cc89d27dc387197772
Source noteuspto-grants-2014_03