HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719383Generated: November 2, 2026
HCID 86760291, compound → HCID 71054124, compound
https://huagongshe.com/reaction/719383
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86760291 | HCID 86760291 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71054124 | HCID 71054124 | — |
Reaction Steps
4-(4Trifluoromethyl-phenyl)-piperazine-1-sulfonic acid ((3R)-1-benzyloxy-2,5-dioxo-pyrrolidin-3-yl)-amid (76 mg; 0.15 mmol) was dissolved in EtOAc (5 ml)+MeOH (5 ml). A slurry of 10% Pd/C (35 mg) in MeOH (1 ml) was added under a stream of nitrogen. The mixture was hydrogenated at room temperature at 1 atm. pressure of H2 for 1 h. The reaction mixture was filtered through celite and the filtercake was washed with EtOAc and MeOH. Evaporation of solvent, the crude product was purified by flash chromatograohy through 10 g of Si-60-gel using a gradient of 100% Heptane to 100% (EtOAc+1% AcOH), gradient time=30 min, then isocratic system 100% (EtOAc+1% AcOH) for 15 min. flow=20 ml/min. The fractions containing the product was evaporated and the residue was trituated with Et2O and the resulting colourless solid was dried to give the title compound. Obtained 47 mg (74% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132434B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-fd378d74fb7941958f0c5b9dd2b124f2 |
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| Source note | uspto-grants-2006_11 |
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