HCID 131728818, compound → HCID 178493032, compound

Participants

Reaction Conditions

Reaction Steps

To a suspension of 4-(6-chloro-2-(2-methoxy-4-morpholinophenyl)-3H-imidazo[4,5-b]pyridin-7-ylamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one (Compound CC) (100 mg, 0.196 mmol) in ethanol NaBH4 (74 mg, 1.96 mmol) was added and the reaction mixture was heated at 60° C. for 16 h when LCMS confirmed consumption of starting material and formation of desired product. The reaction mixture was allowed to come to rt and acidified to pH 5. Solvent was then removed and the residue was suspended in water and filtered. The residue was triturated with ether to afford the desired product (44 mg, 43%) as a light green solid. NMR: δ (1H, 400M Hz, DMSO-d6): 0.89 (3H, s), 0.91 (3H, s), 1.09 (3H, s), 1.00-1.60 (4H, m), 2.70-2.90 (1H, m), 3.20-3.30 (4H, m), 3.60-3.70 (1H, m), 3.70-3.80 (4H, m), 3.97 (3H, s), 5.35 (1H, s), 6.54 (1H, s), 6.74 (1H, d, J=8.8 Hz), 8.03 (2H, d, J=8.8 Hz), 12.26 (1H, s). LCMS (254 nm): [M+H]+ 512.15 (91.18%). HPLC: (254 nm) 89.96% (220 nm)

Provenance & Evidence