HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351739Generated: October 30, 2026
2-Iodoxybenzoic acid → HCID 21099275, compound
https://huagongshe.com/reaction/1351739
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | HCID 21099269 | HCID 21099269 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21099275 | HCID 21099275 | 90% |
Reaction Steps
The mixture of [8-fluoro-1-(2-hydroxy-ethyl)-1-propyl-1,3,4,9-tetrahydro-pyrano[3,4-b]indol-5-yl]-morpholin-4-yl-methanone (100 mg, 0.256 mmol) and o-iodoxybenzoic acid (IBX, 430 mg, 1.54 mmol) in DMSO (3.5 mL) was stirred overnight at room temperature. The solution was diluted with H2O (7 mL) and the precipitates were filtered and the filter cake was rinsed with EtOAc. The filtrate was extracted with EtOAc (3×10 mL) and the combined organic solution was washed with brine (20 mL), dried (Na2SO4) and concentrated. The residue was purified by flash chromatography (silica, 60% EtOAc in hexanes) to give 89 mg (90%) of the title compound as a pale yellow solid. 1H NMR (CDCl3): 300 MHz δ 9.75 (bs, 1H), 9.05 (bs, 1H), 6.89 (m, 2H), 4.00–2.64 (m, 14H), 1.89 (m, 1H), 1.63 (s, 1H), 1.26 (m, 2H), 0.88 (t, J=5.49 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217730B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-0b87b4b10dd6424e864fe90219ef5fd3 |
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| Source note | uspto-grants-2007_05 |
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