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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44402Erstellt: 25. Oktober 2026

4-Methoxybenzylamine → 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile

https://huagongshe.com/reaction/44402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethoxybenzylamineHCID 75452—
Edukt4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrileHCID 2777510—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrileHCID 520031225,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (example 72) (0.66 g, 3.23 mmol) was suspended in DMF (7 mL), and 4-methoxybenzylamine (0.94 mL, 7.26 mmol) was added. The reaction was heated at 100° C. for 1 hour and the DMF was removed under vacuum. The residue was dissolved in TFA (6 mL) and stirred at room temperature for 30 minutes and dichloromethane (10 mL) was added. The solid product that formed was collected, suspended in water and the solution stirred overnight. The solid was collected by filtration to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.150 g, 25%) as a white solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ7.19 (m, 2H), 7.57 (m, 1H), 7.88 (bs, 2H), 8.12 (d, J=7.6 Hz, 1H), 11.23 (s, 1H). MS 186 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541421B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-cce9922a5f3b470095ed458999a01420
Quellennotizuspto-grants-2013_09