Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391165Generated: October 25, 2026

2-Propanone, 1-(acetyloxy)-3-chloro- → (6-Iodoimidazo[1,2-b]pyridazin-2-yl)methanol

https://huagongshe.com/reaction/2391165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanone, 1-(acetyloxy)-3-chloro-HCID 38413—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Iodopyridazin-3-amineHCID 10867834—
SolventEthanolHCID 702—
Product(6-Iodoimidazo[1,2-b]pyridazin-2-yl)methanolHCID 5744104820.1%

Reaction Steps

To a solution of 3-amino-6-iodopyridazine (2.0 g, 9.0 mmol) in ethanol (40 mL) was added 3-chloro-2-oxopropyl acetate (2.73 g, 18.1 mmol), and the mixture was heated under reflux for 24 hr. After cooling the mixture to room temperature, saturated aqueous sodium hydrogencarbonate solution was added to the mixture, and the mixture was extracted with ethyl acetate/tetrahydrofuran. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was collected by filtration and washed with ethyl acetate/hexane to give the title compound (498 mg, 20%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273741B2
Source datasetuspto-grants-2012_09
ORD IDord-fb36066fc9494afc8093712a96d14709
Source noteuspto-grants-2012_09