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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258854Generated: October 26, 2026

Potassium Iodide → 6-chloro-1-{3-[4-(4-fluorobenzoyl)-1-piperidinyl] propyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/258854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
Reactant6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385587—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product6-chloro-1-{3-[4-(4-fluorobenzoyl)-1-piperidinyl] propyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 2142482323%

Reaction Steps

A mixture of 5.6 parts of 6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 4.9 parts of (4-fluorophenyl) (4-piperidinyl) methanone hydrochloride, 8.5 parts of sodium carbonate, 0.2 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. After cooling, water is added and the layers are separated. The 4-methyl-2-pentanone-phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 2-propanol, yielding 1.9 parts (23%) of 6-chloro- 1-{3-[4-(4-fluorobenzoyl)-1-piperidinyl] propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035369
Source datasetuspto-grants-1977_07
ORD IDord-c3d230c344584aacba0c231641c48da9
Source noteuspto-grants-1977_07