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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74234Generated: October 25, 2026

Phenylacetaldehyde → 5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/reaction/74234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
SolventDimethylformamideHCID 6228—
Product5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749808042%

Reaction Steps

To a solution of 5-(benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (200 mg, 0.646 mmol) in dimethylformamide (3 mL) was added phenylacetaldehyde (101 mg, 0.840 mmol) and oxone (258 mg, 0.420 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (110 mg, 42% yield) as light brown amorphous mass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-0bbbe93463ce44a8911d4cac7a6abf1f
Source noteuspto-grants-2014_09