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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 368875Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/368875

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
PatentnummerUS06133446
Quelldatensatzuspto-grants-2000_10
ORD IDord-b9ec82874c98434f919c817e0e47cfa8
Quellennotizuspto-grants-2000_10