HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959667Generated: November 2, 2026
2-Iodoxybenzoic acid → (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(1-methyl-1H-indazol-5-yl)methanone
https://huagongshe.com/reaction/1959667
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(1-methyl-1H-indazol-5-yl)methanol | HCID 58190458 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(1-methyl-1H-indazol-5-yl)methanone | HCID 58190472 | 82.2% |
Reaction Steps
A suspension of (6-chloroimidazo[1,2-b]pyridazin-3-yl)(1-methyl-1H-indazol-5-yl)methanol (13.1) (500.0 mg, 1.60 mmol) and 2-Iodoxybenzoic acid (45%)(1488.0 mg, 2.39 mmol) in 10 mL acetone was heated at reflux for 3 h. Solvent was removed under reduced pressure. The residue was diluted with water; pH was adjusted to around 10 with 10% NaOH aqueous solution. The precipitates were collected by filtration and washed with water three times. The solid was dissolved in DCM, dried over Na2SO4, filtered and concentrated to give the title compound as a white solid (410.0 mg, 78%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 8.46 (s, 1H), 8.42 (m, 1H), 8.32 (m, 1H), 8.27 (d, 1H), 7.95 (dd, 1H), 7.815 (d, 1H), 7.66 (d, 1H), 4.12 (s, 2H). LCMS (method A): [MH]+=312, tR=4.64 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410264B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-4b9dbb0217314a9b9f38407e5f5d7e08 |
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| Source note | uspto-grants-2013_04 |
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