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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Chloro-2-methylimidazo(1,2-b)pyridazine | HCID 10442072 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Chloro-3-iodo-2-methylimidazo[1,2-b]pyridazine | HCID 46941643 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546395B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d38463d02be74aa096fb4a87914febf3 |
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| Source note | uspto-grants-2013_10 |
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