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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7993Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/7993

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 Example 1 (7), 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
PatentnummerUS07087606B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-91f9a9d242cc4d829d962d9a6373321d
Quellennotizuspto-grants-2006_08