Reaktion #957804

Reaktionsgleichung

3-bromo-6-chloroimidazo[1,2-b]pyridazine

2-methoxyethanamine

→

3-bromo-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine

Ausbeute 62.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigepurified by preparative HPLC (neutral)

Vorschrift

A solution of 3-bromo-6-chloroimidazo[1,2-b]pyridazine (844 mg, 3.77 mmol) and 2-methoxyethanamine (1.44 mL) was heated at 170° C. (microwave) for 30 min. The resulting mixture was cooled to room temperature and purified by preparative HPLC (neutral) to afford 3-bromo-N-(2-methoxyethyl)imidazo[1,2-b]pyridazin-6-amine (630 mg, 62% yield) as a off-white solid: 1H NMR (METHANOL-d4) δ: 7.56 (d, J=9.9 Hz, 1H), 7.41 (s, 1H), 6.74 (d, J=9.6 Hz, 1H), 3.62-3.76 (m, 2H), 3.50-3.62 (m, 2H), 3.42 (s, 3H); LRMS (ESI) m/e 271.1 [(M+H)+, calcd for C9H12BrN4O 271.0]

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