HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067586Generated: November 1, 2026
Methyl iodide → 6-Chloro-2-methoxyimidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/1067586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloroimidazo[1,2-b]pyridazin-2-ol | HCID 22989329 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-2-methoxyimidazo[1,2-b]pyridazine | HCID 22989338 | — |
Reaction Steps
2.69 g of 6-chloro-2-hydroxyimidazo[1,2-b]pyridazine was suspended in 30 ml of N,N-dimethylformamide; 838 mg of a 60% sodium hydride dispersion in mineral oil was added little by little, followed by stirring at room temperature for 30 minutes. Under ice water cooling conditions, 1.2 ml of methyl iodide was added, followed by stirring at room temperature for 3 days. Ice water was added, followed by extraction with ethyl acetate; the extract was washed with saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with hexane:ethyl acetate (5:1). The desired fraction was collected and concentrated to yield 1.05 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-ffcf693d184b444e8fcd9a2c420dd100 |
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| Source note | uspto-grants-2001_06 |
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