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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-methoxycarbonyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one | HCID 21991686 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-carboxy-2-isobutyl-6-[4-(methylthio)phenyl)-2H-pyridazin-3-one | HCID 21991639 | 65,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087606B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-91f9a9d242cc4d829d962d9a6373321d |
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| Quellennotiz | uspto-grants-2006_08 |
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