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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 637403Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/637403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiopheneHCID 8030—
EduktPotassium AcetateHCID 517044—
EduktNorastemizole hydrobromideHCID 3018631—
Edukt1-Benzyl-3-piperidone hydrochloride hydrateHCID 3084924—
EduktHCID 178418361HCID 178418361—
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 parts 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 palldium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate 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
PatentnummerUS04556660
Quelldatensatzuspto-grants-1985_12
ORD IDord-8c3a50b0a37c4b588229f06d8f4bbcb9
Quellennotizuspto-grants-1985_12