HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639581Generated: October 26, 2026
Triacetoxyperiodinane → propane-1-sulfonic acid [2,4-difluoro-3-(5H-pyrrolo[2,3-b]pyrazine-7-carbonyl)-phenyl]-amide
https://huagongshe.com/reaction/1639581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | propane-1-sulfonic acid 2,4-difluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl-amide | HCID 58001696 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | propane-1-sulfonic acid [2,4-difluoro-3-(5H-pyrrolo[2,3-b]pyrazine-7-carbonyl)-phenyl]-amide | HCID 44512442 | 77.8% |
Reaction Steps
To propane-1-sulfonic acid 2,4-difluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl-amide (9, 0.243 g, 0.635 mmol), 15 mL of tetrahydrofuran was added, followed by Dess-Martin periodinane (0.270 g, 0.635 mmol). The reaction was allowed to stir at room temperature for 15 minutes, then extracted with ethyl acetate and 5:1 saturated sodium bicarbonate:saturated sodium thiosulfate. The organic layer was dried with anhydrous magnesium sulfate, filtered, and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography eluting with a gradient of 1 to 5% methanol in dichloromethane. The resulting material was re-purified by silica gel column chromatography eluting with a gradient of 10 to 80% ethyl acetate in hexanes. Appropriate fractions were combined and concentrated under vacuum to give the desired compound (P-0001, 188 mg). MS (ESI)[M+H+]+=381.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110576B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-4234c94519e6463a87e11b6797ca5ef9 |
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| Source note | uspto-grants-2012_02 |
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