Ammonium Chloride → HCID 56656269, compound

Participants

Reaction Conditions

Reaction Steps

A solution of 2-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate (221 mg, 0.45 mmol), 6-chloro-4-(5-(4-methylpiperazin-1-yl)pyridin-2-ylamino)-2-methylpyridazin-3(2H)-one (100 mg, 0.30 mmol), potassium phosphate (159 mg, 0.75 mmol) and dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (14.2 mg, 0.03 mmol) in butanol (4 ml) and water (1 mL) was flushed with argon before (bis[dibenzylideneacetone]dipalladium) (8.59 mg, 0.01 mmol) was added and the resulting solution heated at 100° C. in for 2 h. The resulting mixture was cooled, poured into a saturated solution of ammonium chloride and extracted with methylene chloride (2×100 mL). The layers were separated and the organic phase dried over magnesium sulfate. The mixture was filtered and concentrated in vacuo. The residue was dissolved in dioxane (10 mL) and treated with a lithium hydroxide solution (0.5 mL, 2.0 M), and the resulting mixture was stirred at room temperature overnight. The resulting mixture was poured into a saturated ammonium chloride solution and extracted with methylene chloride (2×50 mL). The layers were separated and the organic phase dried over magnesium sulfate. The mixture was filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 24 g, 1% to 14% methanol in dichloromethane) and recrystallized from dichloromethane and isopropyl acetate to give 6-tert-butyl-2-(3-{5-[5-(4-methyl-piperazin-1-yl)-pyridin-2-ylamino]-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yl}-2-hydroxymethyl-phenyl)-8-fluoro-2H-phthalazin-1-one (45 mg, 24%) as a light yellow solid: mp 260-264° C.; 1H NMR (300 MHz, DMSO-d6) δ: ppm 1.38 (s, 9H) 2.20 (s, 3H) 2.33-2.46 (m, 4H) 2.98-3.19 (m, 4H) 3.77 (s, 3H) 4.27-4.69 (m, 3H) 7.24-8.07 (m, 8H) 8.32-8.74 (m, 2H) 9.23 (s, 1H).

Provenance & Evidence