HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356276Generated: October 29, 2026
2-Aminopyridine → Ethyl 2-{imidazo[1,2-a]pyridin-2-yl}acetate
https://huagongshe.com/reaction/356276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-{imidazo[1,2-a]pyridin-2-yl}acetate | HCID 10822054 | 8.4% |
Reaction Steps
A solution of 14.6 g of 2-aminopyridine and 25.5 g of ethyl 4-chloroacetoacetate in 200 ml of acetonitrile was heated under reflux for 14.5 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. The residue thus obtained was mixed with an aqueous solution of potassium carbonate, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent, to give 2.65 g of the title compound having Rf=0.33 (on silica gel thin layer chromatography using ethyl acetate as the developing solvent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834501 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-608034d9cb5f444baafef4e88430ceba |
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| Source note | uspto-grants-1998_11 |
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