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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035787Generated: October 30, 2026

Sodium Thiosulfate → 6-Chloro-3-iodo-2-methylimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1035787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantIodine chlorideHCID 24640—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloro-2-methylimidazo(1,2-b)pyridazineHCID 10442072—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product6-Chloro-3-iodo-2-methylimidazo[1,2-b]pyridazineHCID 46941643—

Reaction Conditions

Temperature0 °C

Reaction Steps

Added to a solution of 7.00 g (41.8 mmol) of 6-chloro-2-methylimidazo[1,2-b]pyridazine (CAS 14793-00-1) in 300 ml of chloroform, cooled to 0° C., are 10.2 g (62.7 mmol) of iodine monochloride in solution in 20 ml of methanol. The reaction is then left at ambient temperature for 16 hours then poured over a mixture of a 5% sodium thiosulphate solution and of sodium hydrogen carbonate. The product is extracted with dichloromethane, the organic phase is dried over sodium sulphate and the solvent is evaporated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546395B2
Source datasetuspto-grants-2013_10
ORD IDord-d38463d02be74aa096fb4a87914febf3
Source noteuspto-grants-2013_10