Potassium Phosphate, Tribasic → Tert-butyl 5-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)isoindoline-2-carboxylate

Participants

Reaction Conditions

Reaction Steps

To a mixture of (6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)boronic acid (47 mg, 0.2 mmol), tert-butyl 5-bromoisoindoline-2-carboxylate (47 mg, 0.16 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (7 mg, 0.01 mmol) and tripotassium phosphate (41 mg, 0.3 mmol) was added 3:1 acetonitrile/water (3 mL). The resulting mixture was heated at 145° C. (microwave) for 800 s. The reaction was then filtered and concentrated. The residue was dissolved in methanol, and then filtered again. The filtration was finally purified by preparative HPLC (neutral) to afford tert-butyl 5-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)isoindoline-2-carboxylate (43 mg, 66% yield) as a white solid: 1H NMR (METHANOL-d4) δ: 8.15 (d, J=10.9 Hz, 1H), 8.00-8.08 (m, 1H), 7.75 (s, 1H), 7.59 (d, J=9.6 Hz, 1H), 7.35 (t, J=9.1 Hz, 1H), 6.68 (d, J=9.9 Hz, 1H), 4.69 (br. s., 4H), 3.37 (d, J=7.3 Hz, 2H), 1.65-1.78 (m, 2H), 1.56 (s, 9H), 1.45-1.53 (m, 2H), 1.02 (td, J=7.3, 2.3 Hz, 3H); LRMS (ESI) m/e 408.3 [(M+H)+, calcd for C23H30N5O2 408.2].

Provenance & Evidence