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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262443Generated: November 3, 2026

HCID 85997294, compound → HCID 23094069, compound

https://huagongshe.com/reaction/2262443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 85997294HCID 85997294—
SolventO-XyleneHCID 7237—
ProductHCID 23094069HCID 2309406969%

Reaction Steps

Suspending 3.1 g (8.4 mmol) of 5′-bromo-2′-(N-phenylamino)-picoline anilide obtained in the above step (1) into 30 milliliter of xylene, and adding 0.48 g (2.5 mmol) of p-toluenesulfonic acid 1 hydrate, the resultant solution was azeotropically dehydrated while refluxing with heating for 5 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 the use of magnesium sulfuric anhydride, followed by removing the solvent by distillation under reduced pressure, 2.0 g of 5-bromo-1-phenyl-2-(2-pyridyl)-1H-benzimidazole was obtained (yield: 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851071B2
Source datasetuspto-grants-2010_12
ORD IDord-ee5d36ae9bec44269b586a6e22dbbe70
Source noteuspto-grants-2010_12