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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1828592Erstellt: 25. Oktober 2026

1-Aminopiperidine → N-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide

https://huagongshe.com/reaction/1828592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-AminopiperidineHCID 16658—
EduktEthyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylateHCID 22066075—
ProduktN-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamideHCID 10183243—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of ethyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylate (50 mg, 0.125 mmol) from Step D in neat 1-aminopiperidine (1 mL) was heated at 90° C. for 72 hr. Most of the amine was evaporated under a stream of nitrogen and the residue was purified by Prep TLC (2×1 mm, silica) (40% ethyl acetate in hexanes to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07057051B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-f44602c857114de3bdbdad2361619324
Quellennotizuspto-grants-2006_06