Reaktionsgleichung
[I:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([NH:11]C(=O)OC(C)(C)C)[N:10]=2)[N:7]=1.Cl.C(OCC)(=O)C.C(OCC)C>C(OCC)(=O)C>[I:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([NH2:11])[N:10]=2)[N:7]=1Komponenten
5
Versuchsvorschrift
To a suspension of tert-butyl (6-iodoimidazo[1,2-b]pyridazin-2-yl)carbamate (10.2 g, 28.3 mmol) in ethyl acetate (50 mL) was added 4N hydrochloric acid/ethyl acetate (75 mL), and the mixture was stirred at room temperature for 4 hr. Diethyl ether (200 mL) was added to the reaction mixture, and the precipitate was filtrated. After washing with saturated aqueous sodium hydrogencarbonate solution, the filtrate was washed with water, acetonitrile and diethyl ether to give the title compound (4.9 g, 67%) as a green powder.
Aufarbeitung
- filtrationthe precipitate was filtrated
- washAfter washing with saturated aqueous sodium hydrogencarbonate solution
- washthe filtrate was washed with water, acetonitrile and diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-7c6ce4cf91e8445499f27372fb85391c
- Quelldatensatz
- uspto-grants-2011_10
- Patentnummer
- US08044049B2
Verknüpfte Notizen
Wird geladen…