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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050300Generated: October 25, 2026

Potassium Iodide → 1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride

https://huagongshe.com/reaction/2050300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
Reactant1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 13360889—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochlorideHCID 20506294—

Reaction Steps

A mixture of 4.94 parts of 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one, 5.76 parts of 1-[bis(4-fluorophenyl)methyl]piperazine, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours with water-separator. After cooling, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from ethanol. The product is filtered off and dried, yielding 1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride. hydrate. hemiethanolate; mp. 172.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-f97ce1a1df92407592231264c8e5ea52
Source noteuspto-grants-1980_04