Reaction Steps
A solution of 2-chloro-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)isonicotinamide (50 mg, 0.12 mmol) in cyclohexylamine (1 ml) was heated at 110° C. for 36 h and then at 160° C. for 48 h in a sealed tube. The reaction was concentrated under vacuum, the residue triturated with water and purified by preparative HPLC. The solvent was evaporated under vacuum to give 2-cyclohexylamino)-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)isonicotinamide (14.4 mg). NMR; δH [2H6]—DMSO 10.26,(1H, s), 8.62,(1H, t), 8.07,(1H, d), 7.92,(2H, d), 7.69-7.66,(2H, m), 7.43,(2H, d), 7.28,(1H, d), 6.84,(2H, m), 6.67,(1H, d), 3.72,(1H, m), 3.16,(2H, t), 2.19,(3H, s), 1.90,(2H, m), 1.70,(2H, m), 1.57,(1H, m), 1.31,(2H, m), 1.18,(3H, m), 1.04,(1H, m), 0.24,(2h, m). LCMS: retention time 3.14 min, MH+483.
