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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167111Erstellt: 26. Oktober 2026

Potassium Carbonate → Methyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylate

https://huagongshe.com/reaction/1167111

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktN-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamideHCID 9928271—
EduktMethyl 6-bromo-2-methyl-2-phenyl-hexanecarboxylateHCID 22995743—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 2-methyl-2-phenyl-6-{4-[(4'-trifluoromethyl-biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-hexanecarboxylateHCID 22995675—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

0.2 g (0.574 mmol) of 4′-trifluoromethyl-biphenyl-2-carboxylic acid-piperidin-4-yl-amide, 0.15 g (0.5 mmol) of methyl 6-bromo-2-methyl-2-phenyl-hexanecarboxylate and 0.083 g (0.6 mmol) of potassium carbonate are dissolved in 10 ml of acetonitrile. The mixture is stirred for 8 hours at 60° C. and for 14 hours at ambient temperature. Then the reaction mixture is poured onto water and extracted with ethyl acetate. The organic phase is dried over sodium sulphate and the solvent is distilled off in the rotary evaporator. After column chromatography on silica gel (eluant: dichloromethane/methanol=20:1) a highly viscous oil remains.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617325B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-6cd803da8c144149904d0fa9c1848818
Quellennotizuspto-grants-2003_09