HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609714Generated: October 30, 2026
HCID 18727129, compound → HCID 18727137, compound
https://huagongshe.com/reaction/609714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18727129 | HCID 18727129 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | HCID 18727137 | HCID 18727137 | 88% |
Reaction Steps
A mixture of 4-(N,N-dimethylaminocarbonyl)-1-[4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine-1-sulfonyl]piperazine-2-(R)-carboxylic acid (1.39 g, 3.16 mmol) [prepared as described in Example 28, Steps 1-4] and 10% Pd/C (0.7 g) in 10% tetrahydrofuran/ethanol (45 ml) was stirred under an atmosphere of hydrogen (1 atm) overnight. The reaction mixture was filtered through Celite with excess ethanol and the filtrate was concentrated in vacuo to give 4-(N,N-dimethylaminocarbonyl)-1-[4-(4-fluorophenyl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxylic acid (88%) as a white solid. This material was converted to N-hydroxy-4-dimethylaminocarbonyl-1-[4-(4-fluorophenyl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxamide by following the procedure described in Example 28, Step 5 above.
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-462d8a80eb064500a11075d53481e5b7 |
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| Source note | uspto-grants-1999_12 |
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