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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80733Generated: October 26, 2026

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

https://huagongshe.com/reaction/80733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantIodine chlorideHCID 24640—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-2-phenyl-HCID 137233—
SolventChloroformHCID 6212—
Product6-Chloro-3-iodo-2-phenylimidazo[1,2-b]pyridazineHCID 2486247192.9%

Reaction Steps

To a solution, cooled to 0° C., of 10.4 g (45.4 mmol) of 6-chloro-2-phenylimidazo[1,2-b]pyridazine (CAS No.: 1844-53-7) in 500 mL of chloroform is rapidly added dropwise a solution of 11.1 g (68.1 mmol) of iodine monochloride in 100 mL of chloroform. After cooling to room temperature and stirring for 1 hour, the mixture is treated with aqueous 5% sodium thiosulfate solution. The product is extracted with dichloromethane and the organic phase is dried over sodium sulfate and concentrated under reduced pressure. The residue is triturated in 150 ml of acetonitrile containing a few mL of isopropyl alcohol and the solid is isolated after filtration. 15 g of a yellow powder are isolated after drying under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846676B2
Source datasetuspto-grants-2014_09
ORD IDord-a6e7b9b5f28f4ac4815b830b87e14950
Source noteuspto-grants-2014_09