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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333928Erstellt: 24. Oktober 2026

Diisopropylethylamine → (E)-1-[4-(2-Methoxy-4-quinolyl)piperazin-1-yl]-4-methyl-hept-2-en-1-one

https://huagongshe.com/de/reaction/333928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt4-Methylhept-2-enoic acidHCID 21720203—
Edukt2-Methoxy-4-piperazin-1-yl-quinolineHCID 66835874—
LösungsmittelDimethylformamideHCID 6228—
Produkt(E)-1-[4-(2-Methoxy-4-quinolyl)piperazin-1-yl]-4-methyl-hept-2-en-1-oneHCID 5694896140%

Reaktionsschritte

(E)-4-Methyl-hept-2-enoic acid (21.3 mg, 0.15 mmol) was dissolved in DMF (350 μl), diisopropylethylamine was added (26 μl, 0.15 mmol) followed by HATU (57 mg, 0.15 mmol dissolved in 0.25 ml DMF). The mixture was stirred at room temperature for 15 minutes, then 2-methoxy-4-piperazin-1-yl-quinoline (36.4 mg, 0.15 mmol, dissolved in 1 ml DMF) was added and stirring was continued overnight. The mixture was evaporated under reduced pressure, the residue was dissolved in dichloromethane and the resulting solution was washed with 5% sodium bicarbonate solution, water, evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 21.1 mg (0.06 mmol, 39.8%) of a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883791B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-32aec6e0d04d40cf81c859d5b8092f64
Quellennotizuspto-grants-2014_11