HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067598Generated: November 2, 2026
Ethyl 2-chloroacetoacetate → Ethyl 6-chloro-2-methylimidazo[1,2-b]pyridazine-3-carboxylate
https://huagongshe.com/reaction/1067598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 6-chloro-2-methylimidazo[1,2-b]pyridazine-3-carboxylate | HCID 14091884 | 12.9% |
Reaction Steps
12.9 g of 3-amino-6-chloropyridazine was suspended in 250 ml of ethanol; 18.1 g of ethyl 2-chloro-3-oxobutanoate was added, followed by thermal refluxing for 6 hours. After cooling, the mixture was concentrated under reduced pressure; the residue was ajusted to pH 7 by the addition of aqueous sodium bicarbonate; ethyl ether was added; the precipitated was collected by filtration and extracted with ethyl ether; the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; ethanol-1 N aqueous solution of sodium hydroxide (1:1) was added; the crystal precipitated was collected by filtration; the filtrate was concentrated again. The residue was crystallized by the addition of ethyl acetate and collected by filtration to yield 3.09 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248740B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-00889c66e5854662b5802d157ae14b44 |
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| Source note | uspto-grants-2001_06 |
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