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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323179Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/323179

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
PatentnummerUS06211199B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-560697a9c71444b5a7705a1b92fc2c32
Quellennotizuspto-grants-2001_04