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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 582054Erstellt: 27. Oktober 2026

2-Chlorobenzimidazole → N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/582054

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-ChlorobenzimidazoleHCID 78572—
Edukt1-Benzyl-4-piperidylamineHCID 415852—
ProduktN-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amineHCID 16640950—

Reaktionsschritte

Combine 2-chloro-1H-benzimidazole (5.0 g, 33 mmol) and 1-benzyl-4-aminopiperidine (14.2 g, 75 mmol) and heat to about 150° C. After 12 hours, cool and partition between water and chloroform, warming if necessary. Separate the layers and add methanol and toluene to the organic layer. Evaporate the organic layer in vacuo to give a solid. Triturate the solid with ethyl acetate, collect by filtration, and dry to give (1H-benzimidazol-2-yl)(1-benzylpiperidin-4-yl)amine: Rf =0.30 (2% triethylamine/10% methanol/ethyl acetate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05922737
Quelldatensatzuspto-grants-1999_07
ORD IDord-d4d8e37fcd0a4bc8977bd503b9a5113f
Quellennotizuspto-grants-1999_07