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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239857Generated: November 1, 2026

HCID 86761113, compound → HCID 59304444, compound

https://huagongshe.com/reaction/2239857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86761113HCID 86761113—
ReactantHCID 178418361HCID 178418361—
CatalystTriethylamineHCID 8471—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59304444HCID 5930444466.7%

Reaction Steps

To a suspension of N-(4-((6-chloroimidazo[1,2-b]pyridazin-8-yl)amino)phenyl)-1-(4-fluorophenyl)-2-oxo-1,2-dihydro-3-pyridinecarboxamide TFA salt (0.013 g, 0.027 mmol) from Example XXI(i) and EtOH (4 mL) in a 500 ml PARR bottle was added 10% Pd/C (20 mg) and 2 drops of triethylamine. The PARR bottle was then charged with Hydrogen gas at 55 psi and allow to shake at room temperature for 12 hours. The reaction mixture was then filtered and the filtrate concentrated in vacuo. The residue was purified by preparative HPLC to furnish 0.008 g of the title compound as a TFA salt. LC/MS, m/e 445 (M+1). HPLC Rt, 1.81 mm. YMC ODSC18 column (4.6×50 mm). 0%-100% B. Solvent B: (90% MeOH, 10% H2O, 0.1% TFA). Solvent A: (10% MeOH, 90% H2O, 0.1% TFA). Gradient, start % B=0, final % B=100, gradient time 4 mm, hold at 100% B 1 mm, flow rate 4 mL/min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-629af5fe654f4409acfcd8470e8d5cef
Source noteuspto-grants-2010_05