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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295775Generated: October 31, 2026

Dimethylformamide → HCID 10112696, compound

https://huagongshe.com/reaction/1295775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
ReactantHCID 16457793HCID 16457793—
SolventWaterHCID 962—
ProductHCID 10112696HCID 1011269666.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

1-[1-(4-Butyl-benzoyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one (197.2 mg, 0.522 mmol), allyl bromide (260 μL, 3.0 mmol) and cesium carbonate (excess) were added to dimethyl formamide (3 mL) and the suspension was stirred at 120° C. in a sealed tube for 72 hours. The reaction was allowed to cool to room temperature and diluted with water (9 mL) then extracted with ethyl ether (2×10 mL). The combined organic phase was dried over sodium sulfate and purified by column chromatography on silica gel using ethyl ether as the eluent. The product fractions were combined and concentrated to give an oily residue. The residue was triturated with ethyl ether and the white crystals that formed were collected by filtration. Vacuum drying yielded 1-allyl-3-[1-(4-butyl-benzoyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one (144 mg, 66%) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244744B2
Source datasetuspto-grants-2007_07
ORD IDord-44629bab4a564b5a82a557c6b3a634ef
Source noteuspto-grants-2007_07