HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359037Generated: November 4, 2026
HCID 86759087, compound → HCID 53990110, compound
https://huagongshe.com/reaction/1359037
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86759087 | HCID 86759087 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53990110 | HCID 53990110 | 98.9% |
Reaction Steps
A mixture of (2R,4R)-2-benzyloxycarbamoyl-1-[3-(4-fluorophenoxy)-propane-1-sulfonyl]-piperidine-4-carboxylic acid methyl ester (800 mg, 1.57 mmol) and 200 mg of 5% palladium on barium sulfate in 15 mL of methanol was shaken in a Parr apparatus under a 40 psi hydrogen gas atmosphere for 2 hours. The catalyst was removed by passage of the mixture through a 0.45 μm nylon filter and the filtrate was concentrated to give 650 mg of (2R,4R)-1-[3-(4-fluorophenoxy)-propane-1-sulfonyl]-2-hydroxycarbamoyl-piperidine-4-carboxylic acid methyl ester as a white foam: MS (atmospheric pressure chemical ionization) acidic mode, 417 (M−1); 1H NMR (400 MHz, CDCl3) δ 6.94-6.97 (m, 2 H), 6.80-6.83 (m, 2 H), 4.56 (s, 1 H), 4.03 (t, 2 H, J=5.3 Hz), 3.83 (d, 1 H, J=12.9 Hz), 3.68 (s, 3 H), 3.15-3.28 (m, 3 H), 2.76 (t, 1 H, J=11.5 Hz), 2.54 (d, 1 H, J=13.5 Hz), 2.26 (d, 2 H, J=5.9 Hz), 2.02 (m, 1 H, J=13.0 Hz), 1.73-1.78 (m, 1 H), 1.56-1.62 (m, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599890B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-60597cd1232d427fa415cd229a6d232a |
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| Source note | uspto-grants-2003_07 |
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