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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419712Generated: October 30, 2026

Potassium Carbonate → 1-Benzyl-4-[5-(3-chloro-4-fluoro-phenyl)-1H-imidazol-2-yl]-piperidine

https://huagongshe.com/reaction/419712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-3'-chloro-4'-fluoroacetophenoneHCID 2782785—
Reactant1-Benzyl-piperidine-4-carboxamidine dihydrochlorideHCID 66649853—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-4-[5-(3-chloro-4-fluoro-phenyl)-1H-imidazol-2-yl]-piperidineHCID 6664980878%

Reaction Conditions

Temperature45 °C

Reaction Steps

Dissolve 1-benzyl-piperidine-4-carboxamidine dihydrochloride (2 g; 1.00 equiv; 6.89 mmoles) in dimethylformamide (90 mL). Add powdered potassium carbonate (4 equiv; 27.56 mmoles; 3.8095 g) and warm to ˜45° C. Add 3-chloro-4-fluoro-phenacyl bromide (2.00 equiv; 13.782 mmoles; 3.5366 g) in 8 mL with DMF dropwise over 40 minutes. Dilute with 50 mL ethyl acetate, stir 5 min and filter. Evaporate and partition with ethyl acetate/sat. sodium bicarbonate, wash organic layer with water, then saturated aqueous sodium chloride. Dry with MgSO4, filter and evaporate to red foam. Purify over flash silica gel with 0-10% MeOH/ACN. Pool fractions to give 1.9772 g (5.346 mmol, 78%) 1-Benzyl-4-[5-(3-chloro-4-fluoro-phenyl)-1H-imidazol-2-yl]-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093383B2
Source datasetuspto-grants-2012_01
ORD IDord-b2e0556a4b61428b852846c57bac4a2b
Source noteuspto-grants-2012_01