Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 605819Erstellt: 25. Oktober 2026

Dimethylformamide → (Pyridin-3-yl) 4-[(6-phenylhexanoyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/605819

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt6-Phenylhexanoic AcidHCID 79695—
EduktSodium BicarbonateHCID 516892—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelWaterHCID 962—
Produkt(Pyridin-3-yl) 4-[(6-phenylhexanoyl)amino]piperidine-1-carboxylateHCID 57507791—

Reaktionsschritte

The resulting compound (0.28 g) was dissolved in dimethylformamide (10 ml), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.28 g), 1-hydroxybenzotriazole (0.16 g), TEA (0.54 ml) and 6-phenylhexanoic acid (0.18 g) were added thereto, followed by stirring at room temperature for 15 hours. Water was added to the reaction solution and further stirred for 1 hour. Then, sodium hydrogencarbonate solution was added thereto, followed by extraction with EtOAc. The organic layer was washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: EtOAc) to obtain a colorless powder. This was recrystallized from methanol and diethyl ether to obtain (pyridin-3-yl) 4-[(6-phenylhexanoyl)amino]piperidine-1-carboxylate (108 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915261B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-6cf816a4115f439daa70a1e171b6341d
Quellennotizuspto-grants-2011_03