Potassium Phosphate, Tribasic → 3-Amino-N-{4-[(3S)-3-aminopiperidin-1-yl]pyridin-3-yl}-7-piperidin-4-ylquinoline-2-carboxamide

Temperature

60 °C

To a screw-cap vial equipped with a magnetic stir bar was added benzyl [(3S)-1-(3-{[(3-{[(benzyloxy)carbonyl]amino}-7-bromoquinolin-2-yl)carbonyl]amino}pyridin-4-yl)piperidin-3-yl]carbamate (56.4 mg, 0.0795 mmol), benzyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridine-1(2H)-carboxylate (Ark Pharm, 48.2 mg, 0.140 mmol), chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II) (Aldrich, 3.2 mg, 0.0041 mmol) and K3PO4 (53.4 mg, 0.252 mmol). The vial was sealed with a Teflon®-lined septum, and was then evacuated and backfilled with nitrogen three times. 1,4-Dioxane (1.00 mL) was added via a syringe, followed by deoxygenated water (0.50 mL). The mixture was heated at 60° C. for 1 h. After cooling to room temperature, the reaction mixture was filtered through a silica gel plug (eluted with MeCN), and concentrated under reduced pressure. The resulting residue was dissolved in MeOH (4.0 mL) and 10 wt % Pd on carbon (43.4 mg, 0.0408 mmol) was added. The mixture was stirred at room temperature under hydrogen (1 atm.) for 15 h. The reaction mixture was then filtered through a pad of diatomaceous earth (eluted with MeOH) and concentrated under reduced pressure. The resulting residue was purified using RP-HPLC (XBridge™ C18 column, eluting with a gradient of MeCN/water containing 0.05% TFA, at a flow rate of 30 mL/min.) to afford the title compound tetrakistrifluoroacetate salt as a yellow solid (13.1 mg, 18%). LCMS calc. for C25H32N7O (M+H)+: m/z=446.3. found 446.2. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 8.98 (s, 1H), 8.97-8.90 (m, 1H), 8.84-8.69 (m, 1H), 8.43 (d, J=6.6 Hz, 1H), 8.31 (s, 2H), 7.74-7.65 (m, 2H), 7.56 (s, 1H), 7.45-7.38 (m, 2H), 3.88-3.76 (m, 1H), 3.59-3.46 (m, 2H), 3.43 (d, J=11.5 Hz, 2H), 3.36-3.25 (m, 2H), 3.13-3.03 (m, 2H), 3.03-2.95 (m, 1H), 2.12-2.03 (m, 3H), 2.03-1.95 (m, 1H), 1.94-1.81 (m, 2H), 1.81-1.65 (m, 2H) ppm.

1. customTo a screw-cap vial equipped with a magnetic stir bar
2. customwas then evacuated
3. addition1,4-Dioxane (1.00 mL) was added via a syringe
4. customby deoxygenated water (0.50 mL)
5. temperatureAfter cooling to room temperature
6. filtrationthe reaction mixture was filtered through a silica gel plug (eluted with MeCN)
7. concentrationconcentrated under reduced pressure
8. dissolutionThe resulting residue was dissolved in MeOH (4.0 mL)
9. filtrationThe reaction mixture was then filtered through a pad of diatomaceous earth (eluted with MeOH)
10. concentrationconcentrated under reduced pressure
11. customThe resulting residue was purified
12. washeluting with a gradient of MeCN/water containing 0.05% TFA, at a flow rate of 30 mL/min.)

ORD record

ord-d3d3dcac41154b628d0cd878c6b742bb

Source dataset

uspto-grants-2016_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09278950B2