HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1663905Erstellt: 24. Oktober 2026
Oxalyl chloride → 1,3-dimethyl-N-{2-methyl-5-[(2-{[(1-methylcyclopropyl)carbonyl]amino}imidazo[1,2-b]pyridazin-6-yl)oxy]phenyl}-1H-pyrazole-5-carboxamide
https://huagongshe.com/de/reaction/1663905
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 1-Methylcyclopropanecarboxylic acid | HCID 81326 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochloride | HCID 57505635 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Lösungsmittel | Tetrahydrofuran ethyl acetate | HCID 21939870 | — |
| Produkt | 1,3-dimethyl-N-{2-methyl-5-[(2-{[(1-methylcyclopropyl)carbonyl]amino}imidazo[1,2-b]pyridazin-6-yl)oxy]phenyl}-1H-pyrazole-5-carboxamide | HCID 57505642 | 74% |
Reaktionsschritte
To a solution of 1-methylcyclopropanecarboxylic acid (97 mg, 0.97 mmol) in tetrahydrofuran (1.5 mL) were added N,N-dimethylformamide (1 drop) and oxalyl chloride (83 μL, 0.97 mmol), and the mixture was stirred at room temperature for 30 min. The reaction mixture was added to a solution of N-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochloride (200 mg, 0.48 mmol) in N,N-dimethylacetamide (5 mL), and the mixture was stirred at room temperature for 1 hr. Ethyl acetate/tetrahydrofuran and saturated aqueous sodium hydrogencarbonate solution were added to the mixture, and the aqueous layer was extracted with ethyl acetate/tetrahydrofuran (×4). Combined organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=30/70→100/0) to give the title compound (105 mg, 74%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08034812B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-bdb26137f96c4213bc52ae8230ed1035 |
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| Quellennotiz | uspto-grants-2011_10 |
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