HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035790Generated: October 31, 2026
Sodium Thiosulfate → 6-Chloro-2-(4-fluorophenyl)-3-iodoimidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/1035790
Participants
| Role | Name | HCID | Charge |
|---|
| 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
A solution of 6.61 g (40.9 mmol) of iodine monochloride in 40 ml of chloroform is added in a rapid dropwise manner 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 number: 244081-70-7) in 130 ml of chloroform. After returning to ambient temperature and after stirring for 4 hours, the mixture is treated with a 5% aqueous solution of sodium thiosulphate. The product is extracted with dichloromethane, the organic phase is dried by filtration over a hydrophobic filtration cartridge and concentrated under reduced pressure. The residue is triturated in acetonitrile, the solid is isolated after filtration and rinsing with diisopropyl ether. 5.7 g of beige powder are isolated after drying under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08546395B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-8a15e145b27f4673a468f9f43dc9cbe5 |
|---|
| Source note | uspto-grants-2013_10 |
|---|