HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846003Generated: October 31, 2026
Sulfuric Acid → 7-ethyl-4-(4-fluoro-3-iodophenyl)-7H-imidazo[4,5-c]pyridazine
https://huagongshe.com/reaction/1846003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3-Diiodo-5,5-dimethylimidazolidine-2,4-dione | HCID 200534 | — |
| Reactant | 7-Ethyl-4-(4-fluorophenyl)-7H-imidazo[4,5-c]pyridazine | HCID 86723231 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-ethyl-4-(4-fluoro-3-iodophenyl)-7H-imidazo[4,5-c]pyridazine | HCID 86723206 | 95% |
Reaction Steps
Concentrated sulphuric acid (10 mL) was carefully added to 7-ethyl-4-(4-fluorophenyl)-7H-imidazo[4,5-c]pyridazine (Preparation 9, 825 mg, 2.4 mmol) surrounded by an ice bath, and the resultant reaction mixture was gently stirred at room temperature until a homogeneous solution was observed. To this was added 1,3-diiodo-5,5-dimethylhydantoin (1.36 g, 3.58 mmol) portion-wise, and stirring was continued for 5 minutes. The viscous mixture was then slowly poured into an aqueous sodium hydroxide solution (1M, 10 mL) at 0° C. with stirring. The black suspension slowly dissolved to give a blue solution. CH2Cl2 (20 mL) was added and the layers were separated. The organic layer was washed with saturated aqueous sodium bisulfite solution (20 mL) then concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with heptane:EtOAc 1:1 to 0:100 to afford the title compound as a white solid in 95% yield, 1.19 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952008B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-a962e7fd7f2347b595d8033b7cbdc197 |
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| Source note | uspto-grants-2015_02 |
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