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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520824Generated: October 31, 2026

Phosphorus oxychloride → 2-(5-bromopyridine-3-yl)-1-phenyl-1H-benzimidazole

https://huagongshe.com/reaction/520824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-bromo-N-(2-(phenylamino)phenyl)nicotinamideHCID 70654227—
Solvent1,4-DioxaneHCID 31275—
Product2-(5-bromopyridine-3-yl)-1-phenyl-1H-benzimidazoleHCID 2309408589%

Reaction Conditions

Temperature100 °C

Reaction Steps

Compound 1E (20.0 g, 54.3 mmol) was dissolved in 1,4-dioxane (anhydrous, 150 mL). Phosphorous oxychloride (36 g, 235 mmol) was then added dropwise. The resulting solution was heated at about 100° C. overnight; solids formed. After cooling to RT, the mixture was poured into hexanes (250 mL) to form additional precipitate. Solids were filtered then redissolved in DCM (200 mL) and washed with potassium carbonate (200 mL, saturated solution). The organic phase was collected, dried over sodium sulfate, and loaded onto silica gel. Short silica plug (20% ethyl acetate in hexanes and precipitation from hexanes gave 16.86 g of Compound 1F; 89% yield, pure by HNMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328094B2
Source datasetuspto-grants-2016_05
ORD IDord-20b39a85af3e49d2ae7fa92bd31b5f13
Source noteuspto-grants-2016_05