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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 620484Erstellt: 25. Oktober 2026

Thiophene → 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/620484

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiopheneHCID 8030—
EduktPotassium AcetateHCID 517044—
EduktNorastemizole hydrobromideHCID 3018631—
Edukt1-Benzyl-3-piperidone hydrochloride hydrateHCID 3084924—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Lösungsmittel2-MethoxyethanolHCID 8019—
Produkt1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amineHCID 13588070—

Reaktionsschritte

A mixture of 25 parts of 1-(phenylmethyl)-3-piperidinone hydrochloride, 55 parts of 1-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-1H-benzimidazol-2-amine dihydrobromide, 1 part of a solution of thiophene in ethanol 4%, 50 parts of potassium acetate and 500 parts of 2-methoxyethanol was hydrogenated at normal pressure and at 50° C. with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filrate was evaporated. The residue was taken up in water and the whole was alkalized with sodium hydroxide. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized twice from acetonitrile. The product was filtered off and dried, yielding 9.75 parts of 1-[(4-fluorophenyl)methyl]-N-[1'-(phenylmethyl)-[1,3'-bipiperidin]-4-yl]-1H-benzimidazol-2-amine; mp. 174.6° C. (intermediate 70).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04820822
Quelldatensatzuspto-grants-1989_04
ORD IDord-7bdfc031db0d40ac90710f30ccf5d574
Quellennotizuspto-grants-1989_04