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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430083Erstellt: 25. Oktober 2026

Diisopropylethylamine → 2-(3-Amino-2-methoxyprop-1-ylamino)-4-methoxyquinoline

https://huagongshe.com/reaction/430083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Methoxypropane-1,3-diamineHCID 9911138—
Edukt2-Chloro-4-methoxyquinolineHCID 12369166—
LösungsmittelMethanolHCID 887—
ProduktAmmoniaHCID 222—
Produkt2-(3-Amino-2-methoxyprop-1-ylamino)-4-methoxyquinolineHCID 1835369136%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 2-chloro-4-methoxyquinoline (1.75 g, 0.00903 mol), 2-methoxy-1,3-propanediamine, bis(trifluoroacetate) (6.00 g, 0.0181 mol) and N,N′-diisopropylethylamine (20 ml) was stirred for 18 h at 110° C. in a sealed reaction tube. After cooling the two phase mixture was diluted in methanol, concentrated onto silica, and then purified by silica gel chromatography (100% dichloromethane, 5%, 10% then 20% (10% 880 aqueous ammonia in methanol) in dichloromethane) to give the title compound as a yellow oil (0.86g, 36%). δH (CD3OD) 3.26-3.56 (4H, m, 2CH2), 3.46 (3H, s, CHOCH3), 3.40-3.60 (1H, m, CHOCH3), 4.02 (3H, s, COCH3), 6.10 (1H, s, 3-H), 7.00-7.81 (4H, m, ArH). MS (ES+) 262 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06320051B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-5802f5090b4446e7803f2b4e2b70c668
Quellennotizuspto-grants-2001_11