HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892782Generated: October 26, 2026
Hydrochloric Acid → Ethyl 2-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-5-oylacetate
https://huagongshe.com/reaction/892782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(2-Methylimidazo[4,5-c]pyrid-1-yl)pyrid-3-oyl chloride | HCID 19877175 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | HCID 178461627 | HCID 178461627 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-5-oylacetate | HCID 54245582 | 63% |
Reaction Steps
Ethyl potassium malonate (57 mg) was suspended in dry tetrahydrofuran (1 ml) and 2M isopropyl magnesium chloride in THF (170 μl) added. The suspension was sonicated for 1/2 hour giving a homogeneous solution. This was added with stirring to the suspension of 6-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-3-oyl chloride in dichloromethane. The mixture was stirred at room temperature for 1/2 hour. It was then poured into 1N hydrochloric acid, stirred for 15 minutes and adjusted to pH8 with saturated sodium bicarbonate. The aqueous phase was extracted with dichloromethane (2×10 ml), the extracts combined, dried over magnesium sulphate and the solvent removed under reduced pressure yielding the title compound as a pale red oil (40 mg, 63%) [as a 1:1 mixture of enol and keto tautomers].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05120747 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-6ce1b905a9144d07b9b8afe97677137b |
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| Source note | uspto-grants-1992_06 |
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