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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 982787Erstellt: 25. Oktober 2026

1-Bromo-2-methylpropane → 4-carboxy-2-isobutyl-6-[4-(methylthio)phenyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/982787

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2-methylpropaneHCID 6555—
EduktPotassium CarbonateHCID 11430—
EduktSodium BicarbonateHCID 516892—
Edukt4-methoxycarbonyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-oneHCID 21991686—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-carboxy-2-isobutyl-6-[4-(methylthio)phenyl)-2H-pyridazin-3-oneHCID 2199163965,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 4-methoxycarbonyl-6-[4-(methylthio)-phenyl]-2H-pyridazin-3-one (8.00 g, 29.0 mmol) in N,N-dimethylformamide (80 mL) were added potassium carbonate (8.02 g, 58.0 mmol) and isobutyl bromide (4.76 g, 34.8 mmol), and the mixture was stirred at 80° C. for 2 hours. The temperature of the reaction mixture was allowed to drop back to room temperature, and a saturated aqueous solution of sodium hydrogencarbonate was added. The mixture was then extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off. Following the procedure of the residue was reacted to yield the title compound as a yellow solid [yield: 65.1% (2 steps)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861428B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-68e83b782cca42b694f834baeaacea16
Quellennotizuspto-grants-2005_03