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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74191Generated: October 23, 2026

3-Pyridinecarboxaldehyde → 5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/en/reaction/74191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749789349.5%

Reaction Steps

5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (0.15 g, 0.484 mmol) was dissolved in DMF (3 mL) and water (0.1 mL), 3-pyridinecarboxaldehyde (0.06 g, 0.561 mmol) was added followed by oxone (0.19 g, 0.310 mmol), and this was stirred at room temperature for 2.5 hours. Aqueous potassium carbonate solution (0.09 g/15 mL) was added to the reaction solution. This was extracted with chloroform, washed with water, and after drying over magnesium sulfate, this was concentrated and purified by silica gel column chromatography. The crystals obtained were washed with hexane and a small amount of ethyl acetate, and dried to yield the title compound (95.0 mg, 49.5% yield) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-897d73089fb64b02b603065e4363a006
Source noteuspto-grants-2014_09