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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095939Generated: October 29, 2026

Diisopropylethylamine → N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)pyridin-2-yl]-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamide

https://huagongshe.com/reaction/2095939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant6-Methyl-2-oxo-1-phenyl-1,2-dihydro-pyridine-3-carboxylic acidHCID 17966630—
ReactantN-{6-[(6-aminopyridin-3-yl)oxy]imidazo[1,2-a]pyridin-2-yl}cyclopropanecarboxamideHCID 58158570—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)pyridin-2-yl]-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamideHCID 5815853852%

Reaction Steps

To a solution of N-{6-[(6-aminopyridin-3-yl)oxy]imidazo[1,2-a]pyridin-2-yl}cyclopropanecarboxamide (200 mg, 0.647 mmol) and 6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylic acid (178 mg, 0.776 mmol) in N,N-dimethylformamide (3 mL) were added N,N-diisopropylethylamine (233 μL, 1.29 mmol) and HATU (320 mg, 0.841 mmol), and the mixture was stirred at room temperature for 6 hr. Ethyl acetate, tetrahydrofuran and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The obtained residue was washed with ethyl acetate and collected by filtration. The obtained white solid was suspended in methyl ethyl ketone (2 mL), and the mixture was stirred at 80° C. for 17 hr. The suspension was collected by filtration to give the title compound (175 mg, 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-146483bc3804462eb25256911c5bd31d
Source noteuspto-grants-2013_05