Ammonium Hydroxide → 3,5-Dichloro-1,4-dihydropyridazin-4-imine
Reaktionsgleichung
[Cl:1][C:2]1[N:3]=[N:4][CH:5]=[C:6]([Cl:9])[C:7]=1Cl.[NH4+:10].[OH-]>CCO>[Cl:1][C:2]1[N:3]=[N:4][CH:5]=[C:6]([Cl:9])[C:7]=1[NH2:10]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
A mixture of 3,4,5-trichloropyridazine (Preparation 3, 500 mg, 2.73 mmole) in EtOH (5.5 mL) and NH4OH (5.5 mL) was heated under microwave irradiation 120° C. for 25 minutes. Concentration under reduced pressure and purification via silica gel column chromatography eluting with acetone:dichloromethane (0-15% acetone), provided the title product in 36% yield, 163 mg.
Aufarbeitung
- concentrationConcentration
- customunder reduced pressure and purification via silica gel column chromatography
- washeluting with acetone
Quellen und Nachweise
- ORD-Eintrag
- ord-684ad457d66744869237a591806839a4
- Quelldatensatz
- uspto-grants-2015_02
- Patentnummer
- US08952008B2
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