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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1417857Erstellt: 26. Oktober 2026

1-benzyl-N-methylpiperidin-4-amine → U 99363

https://huagongshe.com/reaction/1417857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-benzyl-N-methylpiperidin-4-amineHCID 4136128—
Edukt2-BROMO-3-ETHOXYPYRIDINEHCID 10631926—
LösungsmittelDichloromethaneHCID 6344—
ProduktU 99363HCID 133107—

Reaktionsschritte

A mixture of N-(1-benzylpiperidin-4-yl)-N-methylamine (XXVII, 4.80 g) and 2-bromo-3-ethoxypyridine (XXVIIIa, 2.3805 g) is placed in a metal, screw cap reaction vessel using dichloromethane as the transfer solvent. Reduced pressure is applied to the vessel with heating at 50° to 60° for 45 min to remove dichloromethane. The vessel is then sealed and heated at 160° to 165° for 2 days. After cooling, the resulting solids are dissolved in dichloromethane and washed with water and saline. The organic phases are dried over magnesium sulfate and concentrated under reduced pressure to give the product, which is chromatographed (silica gel; eluting with ethyl acetate/hexane (30/70) followed by ethyl acetate/hexane (50/50)), to give N-(1-benzylpiperidin-4-yl)-N-(3-ethoxypyridin-2-yl)-methylamine (XXVIII, Chart G); MS (m/z) 325; IR (neat) 1462, 1211, 1481, 1589 and 1450 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05877317
Quelldatensatzuspto-grants-1999_03
ORD IDord-cc319317b3864991820ceff95256e646
Quellennotizuspto-grants-1999_03