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HRID 7993作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-methylpropaneHCID 6555—
反応物Potassium CarbonateHCID 11430—
反応物Sodium BicarbonateHCID 516892—
反応物4-methoxycarbonyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-oneHCID 21991686—
溶媒DimethylformamideHCID 6228—
生成物4-carboxy-2-isobutyl-6-[4-(methylthio)phenyl)-2H-pyridazin-3-oneHCID 2199163965.1%

反応条件

温度80 °C

反応手順

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)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087606B2
出典データセットuspto-grants-2006_08
ORD IDord-91f9a9d242cc4d829d962d9a6373321d
出典メモuspto-grants-2006_08