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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Reactant | N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide | HCID 57749229 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-({2-[(cyclopropylcarbamoyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-6-methylpyridine-2-carboxamide | HCID 57749386 | 14% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304557B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-a19a567d58f34dd0878b5520b66b0266 |
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| Source note | uspto-grants-2012_11 |
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