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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655288Erstellt: 25. Oktober 2026

Sodium Carbonate → 2-{4-[6-(6-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinolin-3-yl]pyrazol-1-yl}-ethanol

https://huagongshe.com/reaction/655288

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktSodium SulfateHCID 24436—
EduktPotassium AcetateHCID 517044—
Edukt2-(4-Bromo-1H-pyrazol-1-yl)ethanolHCID 16640642—
Edukt3-Bromo-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinolineHCID 59320295—
KatalysatorCID 53485975HCID 53485975—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-{4-[6-(6-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinolin-3-yl]pyrazol-1-yl}-ethanolHCID 59320365—

Reaktionsschritte

To a microwave vessel was added 3-bromo-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinoline (80 mg, 0.23 mmol, 1 equiv), bis(pinacol)borane (69 mg, 0.27 mmol, 1.2 equiv), potassium acetate (66 mg, 0.67 mmol, 3.0 equiv) followed by dimethylacetamide (0.8 mL). The solution was degassed for 10 min and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (7 mg, 0.01 mmol, 0.048 equiv added. The microwave vessel was capped and reacted in a microwave reactor at 120° C. for 1 hour. The microwave vessel was cooled and then 2-(4-bromo-pyrazol-1-yl)-ethanol (0.18 mmol, 0.8 equiv) dissolved in dimethylacetamide (0.6 mL) was added, followed by 2 M aqueous sodium carbonate (0.6 mL). The solution was degassed for 10 min and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (7 mg, 0.01 mmol, 0.048 equiv) added. The microwave vessel was capped and reacted in a microwave reactor at 120° C. for 2 hours. After cooling, Na2SO4 (3 g) was added and the mixture diluted with acetonitrile and filtered through a pad of celite. The filtrate was concentrated onto silica gel and purified by either flash chromatography (SiO2, CH2Cl2:CH3OH 100:0-80:20) or preparative HPLC to return the title compound. Analytical data presented in Table 2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071581B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-d45770956ff34193b9cb446b1c469b32
Quellennotizuspto-grants-2011_12