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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74212Generated: October 31, 2026

2-Thiophenecarboxaldehyde → 5-(Benzoxazol-2-yl)-2-(thiophen-2-yl)-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/reaction/74212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
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-(thiophen-2-yl)-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749828036%

Reaction Steps

5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (0.13 g, 0.42 mmol) was dissolved in DMF (3 mL) and water (0.1 mL), 2-thiophenecarbaldehyde (0.05 g, 0.45 mmol) was added followed by oxone (0.17 g, 0.28 mmol), and this was stirred at room temperature for 2.5 hours. Aqueous potassium carbonate solution (0.10 g/15 mL) was added to the reaction solution. This was extracted with ethyl acetate, 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 (60 mg, 36% yield) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-a987402ca7234d9289113b220d456175
Source noteuspto-grants-2014_09