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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 589097Erstellt: 25. Oktober 2026

Diisopropylethylamine → N-Methoxy-2-pyridin-2-yl-3,4-dihydroquinoline-1(2H)-carboxamide

https://huagongshe.com/reaction/589097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
Edukt4-Nitrophenyl methoxycarbamateHCID 11564735—
Edukt2-Pyridin-2-yl-1,2,3,4-tetrahydroquinolineHCID 90409822—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Methoxy-2-pyridin-2-yl-3,4-dihydroquinoline-1(2H)-carboxamideHCID 9040892795%

Reaktionsschritte

A solution of 2-pyridin-2-yl-1,2,3,4-tetrahydroquinoline (0.723 g, 3.44 mmol) in methylene chloride (10.3 mL) was treated with 4-nitrophenyl methoxycarbamate (0.948 g, 4.47 mmol) (Org. Process Res. Dev. 2012, 16, 109-116) followed by the dropwise addition of N,N-diisopropylethylamine (1.20 mL, 6.88 mmol), and the resulting mixture was stirred at room temperature for 1.5 h. The reaction mixture was then poured over water (25 mL) and saturated sodium bicarbonate (25 mL) and extracted with dichloromethane (2×50 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated to give a crude oily solid. Purification by flash column chromatography (100% hexanes to 20% ethyl acetate/hexanes [the ethyl acetate contained 5% methanol]) gave the desired product (0.923 g, 95%) as a racemic mixture. LCMS calculated for C16H18N3O2 (M+H)+: m/z=284.1. found: 284.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227985B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-ab994f55efbd452aa72be3d56fa76a88
Quellennotizuspto-grants-2016_01