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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397556Erstellt: 23. Oktober 2026

Diisopropylethylamine → 6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/de/reaction/397556

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
EduktSodium BicarbonateHCID 516892—
Edukt4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
Lösungsmittel1-ButanolHCID 263—
Produkt6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415048,8%

Reaktionsschritte

0.464 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine and 1.26 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 20 ml of 1-butanol; 0.62 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 12 hours. After ice water and sodium hydrogen carbonate were added, the reaction mixture was extracted with ethyl acetate; the extract was washed with saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (90:10:1). The desired fraction was collected and concentrated; the crystal obtained was washed with ethyl acetate and dried to yield 0.648 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610694B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-4d3147e3bb5844ada7c54f1b19c9dd47
Quellennotizuspto-grants-2003_08