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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1413508Erstellt: 26. Oktober 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/1413508

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktSodium CarbonateHCID 10340—
Edukt1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
Edukt1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 13360889—
LösungsmittelWaterHCID 962—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produkt1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochlorideHCID 20506294—

Reaktionsschritte

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, 0.2 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours with water-separator. The reaction mixture is cooled, 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; mp. 184.4° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04250176
Quelldatensatzuspto-grants-1981_02
ORD IDord-0300ec4b89324f13b098138029e93880
Quellennotizuspto-grants-1981_02