HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874409Generated: October 25, 2026
Methyl 2-aminopyridine-4-carboxylate → Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate
https://huagongshe.com/reaction/874409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| Reactant | 2-Bromo-1-(2,5-difluorophenyl)ethanone | HCID 2778264 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate | HCID 90383269 | 135.9% |
Reaction Steps
2-Bromo-1-(2,5-difluorophenyl)ethanone (1.5 g) was added to an ethanol (8.2 ml) solution of methyl 2-aminoisonicotinate (1.0 g), and the obtained mixture was then stirred in a nitrogen atmosphere at 60° C. for 18 hours. Thereafter, 2-bromo-1-(2,5-difluorophenyl)ethanone (0.77 g) was added to the reaction solution, and the obtained mixture was then stirred for 6 hours at the same temperature as described above. Thereafter, the reaction solution was concentrated under reduced pressure, and ethyl acetate (10 ml) was then added to the obtained residue. The precipitated solid was collected by filtration, and it was washed with ethyl acetate (15 ml) and heptane (6 ml) and was then dried, so as to obtain the title compound (2.5 g) in the form of a pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980889B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4d7a312991604e409a51268762029261 |
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| Source note | uspto-grants-2015_03 |
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