Hydrochloric Acid → 2-(Aminomethyl)-4-(4-(2-aminopyridin-4-yloxy)-3-fluorophenylamino)-n-(2,4-difluorophenyl)pyrimidine-5-carboxamide, trihydrochloride salt

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Reaction Steps

To a solution of 4-(4-(2-aminopyridin-4-yloxy)-3-fluorophenylamino)-2-cyano-N-(2,4-difluorophenyl)pyrimidine-5-carboxamide, dihydrochloride salt (48 mg, 0.092 mmol) in methanol (1 mL) was added 1 N HCl in ether (30 μL, 0.03 mmol), and 20% palladium hydroxide on carbon (48 mg). The suspension was purged with hydrogen and was stirred 2 h. Additional palladium hydroxide (38 mg) and methanol (1 mL) was added and the mixture was stirred an additional 4 h. The mixture was filtered through Celite® and the filtrate concentrated in vacuo. The resultant residue was purified by preparative (RP) HPLC (gradient from 34% to 90% aqueous methanol with 0.1% TFA). The appropriate fractions were combined and treated with Amberlyst A-21 ion exchange resin, filtered and concentrated in vacuo to give the freebase. The residue was dissolved in anhydrous THF (2 mL), and acidified with 1N HCl in ether. The reaction mixture was stirred for 10 min, the solvent was removed in vacuo and the solid was triturated in ether to afford the amine (20 mg, 39%) as an off-white solid. 1H NMR (DMSO-d6) δ 10.99 (s, 1H), 10.78 (s, 1H), 9.16 (s, 1H), 8.48 (br s, 2H), 8.17 (dd, 1H, J=12.9, 2.4 Hz), 7.99 (d, 1H, J=7.2 Hz), 7.87 (br s, 2H), 7.62 (m, 2H), 7.43 (m, 2H), 7.20 (m, 1H), 6.70 (dd, 1H, J=7.2, 2.4 Hz), 6.21 (d, 1H, J=2.3 Hz), 4.21 (m, 2H); MS(ESI+) m/z 482 (M+H)+.

Provenance & Evidence