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HRID 657875Erstellt: 25. Oktober 2026

1-Butyl-3-methylimidazolium hexafluorophosphate → N*6*,N*6*-Diethyl-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazine-3,6-diamine

https://huagongshe.com/reaction/657875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
Edukt6-Chloro-7,8-dimethyl-[1,2,4]triazolo[4,3-B]pyridazin-3-amineHCID 58045804—
LösungsmittelDiethylamineHCID 8021—
ProduktN*6*,N*6*-Diethyl-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazine-3,6-diamineHCID 58045894—

Reaktionsschritte

6-Chloro-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine (W2.006a, 800 mg and 650 mg divided between 2 microwave vessels) was initially charged each dissolved in 12 ml of diethylamine and admixed with 1-butyl-3-methylimidazolium hexafluorophosphate (150 μl). Subsequently, they were placed into the microwave at 180° C. for 4 h. In order to complete the reaction, they were placed again into the microwave at 180° C. for 4 h and then left to stand overnight. The two reaction mixtures were combined in a round-bottom flask and dried. The residue was admixed with water and extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by means of preparative HPLC (met. F), and the clean product fractions were combined, freed of the acetonitrile under reduced pressure, alkalized with saturated potassium carbonate solution and extracted repeatedly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated. 900 mg of the title compound were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076336B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-cf89ee8961294bbca38c75059dd07309
Quellennotizuspto-grants-2011_12