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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420457Generated: November 1, 2026

O-Xylene → HCID 23094081, compound

https://huagongshe.com/reaction/420457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantHCID 23094082HCID 23094082—
ReactantN-(2-Nitrophenyl)pyridin-2-amineHCID 59785875—
ProductHCID 23094081HCID 2309408167%

Reaction Steps

Suspending 5.5 g (15.0 mmol) of 2-(2-pyridylamino)-4′-bromobenzanilide obtained in the above step (2) into 60 milliliter of xylene, and adding 0.86 g (4.5 mmol) of p-toluenesulfonic acid 1 hydrate, the resultant solution was azeotropically dehydrated while refluxing with heating for 8 hours. The reacted solution was cooled down to room temperature, and the solvent was removed by distillation. Dissolving the resultant solid into ethyl acetate, and after sequentially washing with water, with 10% potassium carbonate aqueous solution and with saturated solution of sodium chloride, it was dried with sulfuric anhydride magnesium, followed by removing the solvent by distillation under reduced pressure, 3.5 g of 1-(2-pyridyl)-2-(4-bromophenyl)-1H-benzimidazole was obtained (yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097349B2
Source datasetuspto-grants-2012_01
ORD IDord-6d4d4d00fc854a2995ae8383b458c7fa
Source noteuspto-grants-2012_01