Potassium Carbonate → 5-(4-(1-Acetylpiperidin-4-yl)phenyl)-6-chloro-1H-indazole-3-carboxylic acid

Temperature

100 °C

A mixture of 5,5,5′,5′-tetramethyl-2,2′-bi-1,3,2-dioxaborinane (110 mg, 0.32 mmol), oven dried potassium acetate (139 mg, 1.41 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (26 mg, 0.032 mmol), and 1-(4-(4-bromophenyl)piperidin-1-yl)ethanone (86 mg, 0.30 mmol) in 1,4-dioxane (3.1 mL) was degassed with N2 for 10 minutes, and subjected to microwave irradiation at 115° C. for 1 hour. The cooled reaction mixture was filtered through cotton and concentrated in vacuo to give a dark solid. To the dark solid was added 5-bromo-6-chloro-1H-indazole-3-carboxylic acid (68.9 mg, 0.25 mmol), 2 N aqueous potassium carbonate solution (0.5 mL, 1.0 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (20.4 mg, 0.025 mmol). The reaction mixture was diluted with degassed toluene (0.8 mL) and EtOH (0.8 mL), sealed in a pressure tube and heated at 100° C. for 1 hour then 75° C. for an additional 16 hours. The cooled reaction mixture was concentrate in vacuo, and the residue was partitioned between 0.5 N HCl (14 mL) and EtOAc (15 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×8 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The resulting reddish solid was purified by reverse phase HPLC Column: Waters XBridge C18 19×100 mm, 5 μm; Mobile phase A: 0.03% NH4OH in water (v/v); Mobile phase B: 0.03% NH4OH in MeCN (v/v); 85.0% H2O/15.0% MeCN linear to 65.0% H2O/35.0% MeCN in 10.5 min, 65.0% H2O/35.0% MeCN linear to 0% H2O/100% MeCN in 0.5 min HOLD at 0% H2O/100% MeCN from 11.0 to 12.0 min. Flow: 25 mL/min) to give the title compound (14.4 mg, 15% yield). MS (ES+) 398.2 (M+H)+. Retention time=2.55 minutes (Column: Waters Atlantis dC18 4.6×50 mm, 5 μm; Mobile phase A: 0.05% TFA in water (v/v); Mobile phase B: 0.05% TFA in MeCN (v/v); Gradient: 95:5 A:B linear to 5:95 A:B in 4.0 min, hold at 5:95 A:B to 5.0 min. Flow: 2 mL/min).

1. customwas degassed with N2 for 10 minutes
2. customirradiation at 115° C. for 1 hour
3. customThe cooled reaction mixture
4. filtrationwas filtered through cotton
5. concentrationconcentrated in vacuo
6. customto give a dark solid
7. customsealed in a pressure tube
8. customThe cooled reaction mixture
9. concentrationwas concentrate in vacuo
10. customthe residue was partitioned between 0.5 N HCl (14 mL) and EtOAc (15 mL)
11. customThe layers were separated
12. extractionthe aqueous layer was extracted with EtOAc (3×8 mL)
13. dry with materialThe combined organic layers were dried over Na2SO4
14. concentrationconcentrated in vacuo
15. customThe resulting reddish solid was purified by reverse phase HPLC Column
16. wait85.0% H2O/15.0% MeCN linear to 65.0% H2O/35.0% MeCN in 10.5 min
17. wait65.0% H2O/35.0% MeCN linear to 0% H2O/100% MeCN in 0.5 min HOLD at 0% H2O/100% MeCN from 11.0 to 12.0 min

ORD record

ord-20d06bd3f5864afdae644c62e9ba7039

Source dataset

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09394285B2