HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942050Generated: November 2, 2026
Iodide Ion → 6-Chloro-3-(1-(6-fluoro-1-methyl-1H-indazol-5-yl)ethyl)imidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/1942050
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)-1-(6-fluoro-1-methyl-1H-indazol-5-yl)ethanol | HCID 58147540 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Chloro-3-(1-(6-fluoro-1-methyl-1H-indazol-5-yl)ethyl)imidazo[1,2-b]pyridazine | HCID 58147517 | — |
Reaction Steps
(rac)-1-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(6-fluoro-1-methyl-1H-indazol-5-yl)-ethanol ((i), 21.4 g, 61.9 mmol) was dissolved in acetic acid (310 mL) and introduced in 20 microwave reactor-vials. Iodide (2.36 g×20, 186 mmol), followed by H3PO2 50% (2.56 mL×20, 464 mmol) were then added into each vial. Then they were submitted to microwave irradiations 10 min at 150° C. The combined RMs were concentrated in vacuo and the residue was diluted with water, basified by a 4 M NaOH solution and extracted twice with EtOAc. The organics were joined and washed with brine, dried over Na2SO4 and the solvent was removed. The residue was triturated with diisopropyl ether. The precipitate formed was filtered off to give a beige solid (tR 4.08 min (conditions 1), tR 14.39/16.40 min (conditions 2), MH+=330, 1H-NMR in DMSO-d6: 8.19 (d, 1H); 7.92 (s, 1H); 7.80 (s, 1H); 7.55 (d, 1H); 7.42 (d, 1H); 7.28 (d, 1H); 4.84 (m, 1H); 3.96 (s, 3H); 1.71 (d, 3H)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389526B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-625ea207a68c49ef83b96d2105d3e908 |
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| Source note | uspto-grants-2013_03 |
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