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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73795Generated: October 30, 2026

Potassium Phosphate, Tribasic → 5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamide

https://huagongshe.com/reaction/73795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 11587208—
Reactant(R)-5-Bromo-N-(4-(1,1-difluoroethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamideHCID 86702628—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamideHCID 131731838—

Reaction Conditions

Temperature110 °C

Reaction Steps

K3PO4 (113 mg, 0.532 mmol), 1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (99 mg, 0.355 mmol) and Pd(PPh3)4 (10.24 mg, 8.86 mmol) were added to a solution of (R)-5-bromo-N-(4-(1,1-difluoroethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamide (Stage 30.1, 80 mg, 0.177 mmol) in toluene (1.5 mL) under argon atmosphere. and the RM was stirred at 110° C. for 1 h. The RM was diluted with EtOAc (20 mL) treated with sat. NaHCO3 solution (20 mL). and extracted with EtOAc. The combined extracts were washed with brine (20 mL), dried with Na2SO4 and the solvent was evaporated off under reduced pressure to give a crude product which was purified by flash chromatography (Silica gel column, 12 g DCM/EtOH from 97:3 to 95:5) to afford N-(4-(1,1-difluoroethoxy)phenyl)-6-(R)-3-hydroxypyrrolidin-1-yl)-5-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)nicotinamide which (66 mg, 0.129 mmol) was dissolved in DCM (1.5 mL) and treated with TFA (0.546 mL, 7.09 mmol) and stirred for 2 h at RT. The RM was diluted with EtOAc (20 mL), treated with sat. NaHCO3 solution (25 mL) and extracted with EtOAc (20 mL). The combined extracts were washed with brine (20 mL), dried over Na2SO4 and the solvent was evaporated off under reduced pressure to give the crude product which was purified by preparative HPLC (Condition 10). Fractions containing pure product were combined, treated with 0.5 g NaHCO3 and the MeCN was evaporated off under reduced pressure. The aq. residue was extracted with DCM to give the title product as a white solid. HPLC (Condition 5) tR=5.42 min, UPLC-MS (Condition 3) tR=0.82 min, m/z=430.1 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 1.68-1.87 (m, 2H) 1.93 (t, J=13.67 Hz, 3H) 2.94 (d, J=11.71 Hz, 1H) 3.15-3.33 (m, 2H) 3.38-3.48 (m, 1H) 4.19 (br. s, 1H) 6.37 (s, 1H) 7.15 (d, J=9.37 Hz, 2H) 7.65-7.83 (m, J=9.37 Hz, 3H) 8.03 (d, J=2.34 Hz, 1H) 8.73 (d, J=2.34 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829195B2
Source datasetuspto-grants-2014_09
ORD IDord-c8e126c84600462fb854bf83dde7d6b3
Source noteuspto-grants-2014_09