HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698147Generated: October 29, 2026
HCID 59278512, compound → HCID 59278338, compound
https://huagongshe.com/reaction/1698147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59278512 | HCID 59278512 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59278338 | HCID 59278338 | — |
Reaction Steps
To a room temperature solution of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-3,4-dihydroxy-1-(2-methanesulfonyl-pyridin-4-yl)-butyl]-amide (0.710 g, 1.42 mmol) in acetone (18 mL) and water (9 mL) was added NaIO4 (608 mg, 2.84 mmol). After 18 hours, the mixture was filtered through diatomaceous earth washing with acetone (3×20 mL). The acetone was removed in vacuo and the aqueous layer was diluted with brine (50 mL) and extracted with EtOAc (3×50 mL). The combined organics layers were dried over magnesium sulfate, filtered, and evaporated to afford 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-1-(2-methanesulfonyl-pyridin-4-yl)-3-oxo-propyl]amide as white solid which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163918B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-403f9424cc744b89bc3bb2c2d059205c |
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| Source note | uspto-grants-2012_04 |
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