HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456090Generated: October 30, 2026
Iodine → 6-Chloro-3-[1-(4,6-difluoro-1-methyl-1H-indazol-5-yl)-ethyl]-imidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/456090
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | 1-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(4,6-difluoro-1-methyl-1H-indazol-5-yl)-ethanol | HCID 58147529 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Chloro-3-[1-(4,6-difluoro-1-methyl-1H-indazol-5-yl)-ethyl]-imidazo[1,2-b]pyridazine | HCID 58147539 | 63.2% |
Reaction Steps
A solution of 1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(4,6-difluoro-1-methyl-1H-indazol-5-yl)-ethanol (530 mg, 1.457 mmol), Iodine (925 mg, 3.64 mmol) and phosphinic acid (50%, 0.556 mL) in 20 mL acetic acid was heated at 110° C. for 2 hours. Solvent was evaporated and the residue was dissolved in water, neutralized with sat. NaHCO3 solution and extracted with CH2Cl2 for three times. Organic layers were combined and washed with brine, dried over Na2SO4. Solvent was then evaporated and the crude was purified on flash chromatography (Hexane:EtOAc 1:2) to give the title compound as a light yellow solid (320 mg, 63.2%). 1H-NMR (400 MHz, MeOH-d4) δ ppm 8.03 (s, 1H), 8.0 (d, 1H), 7.8 (s, 1H), 7.23 (d, 1H), 7.19 (d, 1H), 5.1 (q, 1H), 4.0 (s, 3H), 1.92 (d, 3H). LCMS (method B): [MH]+=347.9, tR=2.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497368B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8151c49b386e4e93a68f1e7890c3848a |
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| Source note | uspto-grants-2013_07 |
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