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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874550Generated: October 27, 2026

Cyclopropylamine → N-[3-({2-[(cyclopropylcarbamoyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-6-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1874550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantN-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamideHCID 57749229—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-({2-[(cyclopropylcarbamoyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-6-methylpyridine-2-carboxamideHCID 5774938614%

Reaction Steps

To a solution of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide (300 mg, 0.835 mmol) and N,N-diisopropylethylamine (286 μL, 1.67 mmol) in tetrahydrofuran (5 mL) was added 2,2,2-trichloroethylchlorocarbonate (130 μL, 0.944 mmol), and the mixture was stirred at room temperature for 50 min. N,N-Dimethylformamide (5 mL) and cyclopropaneamine (290 μL, 4.19 mmol) were added to the reaction mixture, and the mixture was stirred at 80° C. for 11 hr. The reaction mixture was concentrated under reduced pressure, diluted with aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (0%→100% ethyl acetate-hexane) to give the title compound (51.0 mg, 14%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-a19a567d58f34dd0878b5520b66b0266
Source noteuspto-grants-2012_11