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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15339Erstellt: 23. Oktober 2026

Ammonium Bicarbonate → (cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide

https://huagongshe.com/de/reaction/15339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium BicarbonateHCID 14013—
EduktHOAtHCID 181649—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt(cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium saltHCID 131728173—
LösungsmittelDimethylformamideHCID 6228—
Produkt(cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamideHCID 68684194109,6%

Reaktionsschritte

To a solution of (cis)-4-hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium salt (17 g) and 1-hydroxy-7-azabenzotriazole (5 g, 37 mmol) in N,N-dimethylformamide was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (14.1 g, 73.4 mmol), followed by ammonium bicarbonate (21 g, 26.6 mmol). The reaction mixture was stirred at room temperature for 18 h. The solvent was then removed under reduced pressure and the residue was treated with aqueous sodium bicarbonate solution. The aqueous phase was extracted with 9:1 dichloromethane:methanol mixture. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel using a methanol and dichloromethane gradient (0-20% methanol/dichloromethane). This provided the desired compound (9.5 g, 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732461B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-52297c47cb074e87971b38222413d726
Quellennotizuspto-grants-2010_06