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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513309Generated: October 31, 2026

3-Pyridinylboronic acid → HCID 67502008, compound

https://huagongshe.com/reaction/513309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant4-(2,3-Difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamideHCID 67500438—
CatalystCupric acetateHCID 8895—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 67502008HCID 67502008—

Reaction Steps

The mixture of 4-(2,3-difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamide (Example 209) (100 mg, 0.21 mmol), 3-pyridineboronic acid (265 mg, 2.10 mmol), Cu(OAc)2 powder (190 mg, 1.05 mmol) in 5 mL DCM and 1 mL pyridine was stirred at RT for 2 days. It was diluted with methanol and filtered through celite. The filtrate was treated with TFA and concentrated in vacuo. The residue was subjected to reverse phase HPLC to isolate the title compound. MS found for C29H28F2N6O as (M+H)+ 515.5. UV: λ=268 nm. 1H NMR: (CD3OD) δ 8.41 (1H, m), 8.16 (1H, s), 8.09 (1H, s), 8.06 (1H, s), 7.81 (1H, m), 7.35 (2H, dt, J=8.4; 2.0 Hz), 7.24 (1H, m), 7.16 (1H, m), 7.12-7.07 (3H, m), 5.79 (1H, s), 4.55 (2H, s), 4.12 (2H, m), 3.13 (2H, m), 2.91 (1H, m), 2.04 (2H, m), 1.87 (2H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102625B2
Source datasetuspto-grants-2015_08
ORD IDord-369733ed42884049bbef3658374b03ac
Source noteuspto-grants-2015_08