HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609694Generated: October 29, 2026
HCID 18727257, compound → HCID 18727204, compound
https://huagongshe.com/reaction/609694
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 18727257 | HCID 18727257 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | HCID 18727204 | HCID 18727204 | 96% |
Reaction Steps
A solution of N-benzyloxy-4-(N,N-dimethylaminocarbonyl)-1-[4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxamide (8.90 g, 13.97 mmol) [prepared as described in Step 6 above] in argon deoxygenated 80% ethanol/tetrahydrofuran (470 ml) was treated with 10% Pd/C (3.5 g) and stirred under a hydrogen atmosphere (1 atm) for 45 min. The reaction was degassed under argon, filtered through Celite, and the filtrate was concentrated in vacuo. Ethyl acetate (5 ml) was added and the solution was added dropwise to hexane (250 ml) with vigorous stirring. The solid was filtered to afford N-hydroxy-4-(N,N-dimethylaminocarbonyl)-1-[4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxamide (96%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998412 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-f73323852e6a442d96fb580168fd0c6a |
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| Source note | uspto-grants-1999_12 |
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