HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361279Generated: October 30, 2026
HCID 59278246, compound → HCID 59278428, compound
https://huagongshe.com/reaction/1361279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59278246 | HCID 59278246 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 59278428 | HCID 59278428 | — |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid {(S)-1-[2-(1-hydroxy-ethyl)-pyridin-4-yl]-propyl}-amide (71 mg, 0.17 mmol) in acetone (4 mL) was added MnO2 (147 mg, 1.69 mmol). After 18 hours, the reaction was monitored by HPLC-MS indicating a 1:3 mixture of product to starting material. The mixture was filtered through diatomaceous earth rinsing with acetone (200 mL) and the filtrate was concentrated in vacuo. The residue was diluted with acetone (4 mL) and MnO2 (147 mg, 1.69 mmol) was added. After 5 hours, the reaction was filtered through diatomaceous earth, rinsed with acetone and the filtrate was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with using a gradient of 10-100% EtOAc in heptane to afford 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-1-(2-acetyl-pyridin-4-yl)-propyl]amide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879873B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-0b75e251b61541c78c30de219c07073d |
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| Source note | uspto-grants-2011_02 |
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