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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | 6-Chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazine | HCID 11436572 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Chloro-2-(4-fluorophenyl)-3-iodoimidazo[1,2-b]pyridazine | HCID 58046367 | 72.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354405B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-471ec68d71cd44ec9d7cd447d827b676 |
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| Source note | uspto-grants-2013_01 |
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