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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 734492Erstellt: 24. Oktober 2026

Ammonium Chloride → 3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline

https://huagongshe.com/de/reaction/734492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2-Methyl-5-(4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinolineHCID 49851902—
KatalysatorIronHCID 23925—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}anilineHCID 4985210584%

Reaktionsschritte

A solution of 2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline (D5) (0.14 g; 1 eq) in methanol (3 mL) was added dropwise to a suspension of iron powder (0.07 g; 3.2 eq) and ammonium chloride (0.1 g; 5.3 eq) in water (3 mL). The reactants were heated at reflux for 8 hours, adding additional amounts of iron powder (total 0.07 g; 3.2 eq) and ammonium chloride (total 0.1 g; 5.03 eq) in 3 portions during the reaction. The reaction mixture was filtered using a Millipore filter. The filtrate was concentrated under reduced pressure, diluted with water (5 mL) and a saturated aqueous solution of sodium hydrogen carbonate (2 mL), extracted into ethyl acetate (3×5 mL), dried over Na2SO4 and concentrated under reduced pressure obtaining the title compound in 84% yield (0.11 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592346B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-9cc5eea985ac4dcfbc1442cd2f95c9c8
Quellennotizuspto-grants-2009_09