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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803898Generated: November 1, 2026

Sodium Thiosulfate → 6-Chloro-2-(4-fluorophenyl)-3-iodoimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1803898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantIodine chlorideHCID 24640—
Reactant6-Chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazineHCID 11436572—
SolventChloroformHCID 6212—
Product6-Chloro-2-(4-fluorophenyl)-3-iodoimidazo[1,2-b]pyridazineHCID 5804636772.7%

Reaction Steps

To a solution, cooled to 0° C., of 5.20 g (21.0 mmol) of 6-chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazine (CAS No.: 244081-70-7) in 130 mL of chloroform is rapidly added dropwise a solution of 6.61 g (40.9 mmol) of iodine monochloride in 40 mL of chloroform. After cooling to room temperature and stirring for 4 hours, the mixture is treated with aqueous 5% sodium thiosulfate solution. The product is extracted with dichloromethane. The organic phase is dried by filtration through a hydrophobic filter cartridge and concentrated under reduced pressure. The residue is triturated in acetonitrile, and the solid is isolated after filtering off and rinsing with diisopropyl ether. 5.7 g of a beige-colored powder are isolated after drying under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354405B2
Source datasetuspto-grants-2013_01
ORD IDord-471ec68d71cd44ec9d7cd447d827b676
Source noteuspto-grants-2013_01