HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361136Generated: October 30, 2026
HCID 59278146, compound → HCID 59278390, compound
https://huagongshe.com/reaction/1361136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59278146 | HCID 59278146 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59278390 | HCID 59278390 | — |
Reaction Steps
A mixture of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-1-(2-bromopyridin-4-yl)-propyl]amide (165 mg, 0.363 mmol) and 10% palladium on carbon (77 mg) in ethanol (10 mL) was placed under 1 atmosphere of hydrogen (balloon). After 16 hours, diatamacous earth (300 mg) was added and the mixture and the solution was filtered through diatamacous earth and concentrated to afford an oil. The crude material was dissolved in a 4:1 mixture of acetonitrile in water and purified by reversed-phase HPLC. The desired fractions from the column were concentrated to remove the acetonitrile, diluted with saturated aqueous sodium bicarbonate and extracted with dichloromethane. The organic phase was dried over sodium sulfate and concentrated to afford the title compound.
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-13eab9e0bed14bfc8494b9eef926d28b |
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| Source note | uspto-grants-2011_02 |
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