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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959635Generated: November 1, 2026

Sodium Iodide → 1-(6-Chloroimidazo(1,2-b)pyridazin-3-yl)ethan-1-one

https://huagongshe.com/reaction/1959635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChloroacetoneHCID 6571—
Reactant[2-(6-Chloro-3-pyridazinyl)-2-azavinyl]dimethylamineHCID 6802247—
SolventDimethylformamideHCID 6228—
Product1-(6-Chloroimidazo(1,2-b)pyridazin-3-yl)ethan-1-oneHCID 1324880551.1%

Reaction Conditions

Temperature80 °C

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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410264B2
Source datasetuspto-grants-2013_04
ORD IDord-5ed6fe80c0e9481cbb59b69e22977290
Source noteuspto-grants-2013_04