HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497451Generated: October 29, 2026
HCID 69748793, compound → HCID 69748878, compound
https://huagongshe.com/reaction/497451
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 69748793 | HCID 69748793 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69748878 | HCID 69748878 | 97% |
Reaction Steps
In a dry 500-mL Paar flask charged with 10 wt % palladium on carbon (0.050 g) and (3R,4R)-4-benzyloxycarbonylamino-3-[(S)-3-(4-fluoro-benzyl)-piperidine-1-carbonyl]-piperidine-1-carboxylic acid t-butyl ester (0.25 g, 0.451 mmol) was added methanol (15 mL). The reaction mixture was hydrogenated at 48 psi for 18 hours with vigorous shaking. The reaction mixture was filtered through a plug of celite. The plug was washed with 20 mL of methanol and the combined filtrates were concentrated in vacuo to give a white solid (0.183 g, 97%). 1H NMR (300 MHz, CDCl3), δ: 8.11 (bs, 2H), 7.15 (m, 2H), 6.97 (t, 2H, J=8), 4.23 (bm, 3H), 3.88 (m, 1H), 3.67 (bs, 1H), 3.13 (m, 1H), 2.60 (bm, 5H), 2.31 (bd, 1H, J=12), 1.74 (bm, 6H), 1.47 (2s, 9H), 1.20 (m, 1H). MS (ESI), m+/z: (M+H)+=420.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949546B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-2ed6bbf5e8404cd3ba2db3751998e832 |
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| Source note | uspto-grants-2005_09 |
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