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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348652Erstellt: 25. Oktober 2026

Sodium Hydroxide → N-(4-dipropylaminomethylphenyl)-4-{[(1H-imidazol-2-ylmethyl)-quinolin-4-ylmethylamino]-methyl}-benzamide

https://huagongshe.com/reaction/348652

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt4-QuinolinecarboxaldehydeHCID 78072—
EduktSodium cyanoborohydrideHCID 5003444—
EduktN-[4-(dipropylamino)phenyl]-4-[(1H-imidazol-2-ylmethylamino)methyl]benzamideHCID 21084514—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
ProduktN-(4-dipropylaminomethylphenyl)-4-{[(1H-imidazol-2-ylmethyl)-quinolin-4-ylmethylamino]-methyl}-benzamideHCID 10099349—

Reaktionsschritte

The compound (104.9 mg) obtained in Example 47-3 was dissolved in methanol (3.2 ml) and then added with quinoline-4-aldehyde (47.2 mg) and sodium cyanoborohydride (31.4 mg). Then, the solution was adjusted to pH 5 with acetic acid and then stirred at room temperature for 14 hours. After completion of the reaction, a 1 mol/l sodium hydroxide aqueous solution was added to the reaction solution, followed by separation/extraction with chloroform. The organic layer was dried with anhydrous sodium sulfate and the solvent was then distilled off. The residue was purified through silica gel column chromatography (chloroform/ethyl acetate) and then treated with hydrochloric acid, thereby obtaining hydrochloride (76.4 mg) of the subject compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176227B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-95db98f9488c42be844123b91bbabb06
Quellennotizuspto-grants-2007_02