HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456044Generated: October 25, 2026
Sodium Iodide → 1-(6-Chloroimidazo(1,2-b)pyridazin-3-yl)ethan-1-one
https://huagongshe.com/reaction/456044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | [2-(6-Chloro-3-pyridazinyl)-2-azavinyl]dimethylamine | HCID 6802247 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(6-Chloroimidazo(1,2-b)pyridazin-3-yl)ethan-1-one | HCID 13248805 | 51.1% |
Reaction Steps
To a solution of N′-(6-chloro-pyridazin-3-yl)-N,N-dimethyl-formamidine (1.3 g, 7 mmol) in DMF (60 mL) was added NaI (1 g, 6.7 mmol) and chloroacetone (1 mL, 12.6 mmol). The mixture was heated at 80° C. overnight and then concentrated under reduced pressure. The residue was purified by column chromatography to afford 1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-ethanone (0.7 g) in 51% yield. 1H-NMR (400 MHz, CDCl3) δ ppm 8.42 (s, 1H), 8.05 (d, 1H), 7.31 (d, 1H), 2.77 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497368B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-81f316cd6c6748b095ca0bfe48814ec7 |
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| Source note | uspto-grants-2013_07 |
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