Chloroacetone → 6-Chloro-2-methylimidazo(1,2-b)pyridazine
Reaktionsgleichung
[Cl:1][C:2]1[N:7]=[N:6][C:5]([NH2:8])=[CH:4][CH:3]=1.Cl[CH2:10][C:11](=O)[CH3:12].C(N(CC)CC)C>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:10]=[C:11]([CH3:12])[N:8]=2)[N:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 150 °C
Versuchsvorschrift
To a solution of 6-chloropyridazin-3-amine (2.35 g, 18.1 mmol, 1.0 equiv) in ethanol (15 mL) was added 1-chloropropan-2-one (2.92 mL, 36.3 mmol, 2.0 equiv) and triethylamine (2.53 mL, 18.1 mmol, 1.0 equiv). The solution was heated at 150° C. for 30 min then quenched with water. Purification by column chromatography using 30% ethyl acetate in hexanes elution gave 2.43 g of the brown solid, 80%.
Aufarbeitung
- customthen quenched with water
- customPurification by column chromatography
- wash30% ethyl acetate in hexanes elution
Quellen und Nachweise
- ORD-Eintrag
- ord-0d9a4f03b8304040ba63a17d87d5f7ab
- Quelldatensatz
- uspto-grants-2016_06
- Patentnummer
- US09370515B2
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