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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323183Erstellt: 24. Oktober 2026

Ethyl 4-amino-1-piperidinecarboxylate → (1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amine

https://huagongshe.com/de/reaction/323183

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Edukt2-chloro-1-(2-ethoxyethyl)-1H-benzimidazoleHCID 10489356—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amineHCID 22009481—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

Combine 1-(2-ethoxyethyl)-2-chloro-1H-benzimidazole (3.06 g, 13.62 mmol) and ethyl 4-aminopiperidine-1-carboxylate (5.16 g, 30 mmol) and heat to 150° C. After 12 hours, heat to 170° C. After 8 hours, cool the reaction mixture and partition between dichloromethane (150 mL) and water. Separate the layers and extract the organic layer with water. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate/hexane 1/1 to give (1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amine: Rf=0.15 (silica gel, ethyl acetate/hexane).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211199B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-f5b1e0492c1340f09d2a6f9c5b78700a
Quellennotizuspto-grants-2001_04