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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 83646Erstellt: 24. Oktober 2026

Sodium hydride → HCID 66571463, Verbindung

https://huagongshe.com/de/reaction/83646

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktEthanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
EduktN-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamideHCID 66571403—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 66571463HCID 66571463—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

N-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide (50 mg, 0.133 mmol) dissolved in 0.5 mL of DMF was added to a suspension of sodium hydride (7.99 mg, 0.200 mmol) in 1.0 mL of DMF. The reaction was heated at 70° C. for ten minutes before adding 2-methoxyethyl 4-methylbenzenesulfonate (0.144 mL, 0.266 mmol). The reaction was allowed to stir overnight. After 18 hours, the reaction was cooled to room temperature before diluting with water and ethyl acetate. The organic phase was washed with water followed by saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated. The crude material was purified via column chromatography using 50-80% ethyl acetate/hexanes. The purification provided product as a white solid 1H-NMR (400 MHz, DMSO-d6) 7.63-7.49, 7.43-7.14, 7.12-7.03, 6.67-6.58, 4.68, 4.63-4.06, 3.53, 3.20-3.13, 3.10-2.92, 2.79, 1.92-1.50

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846684B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d3af2161ee3b470897c7471e4f176c77
Quellennotizuspto-grants-2014_09