HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362833Generated: October 29, 2026
HCID 59898559, compound → HCID 59898565, compound
https://huagongshe.com/reaction/1362833
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59898559 | HCID 59898559 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59898565 | HCID 59898565 | — |
Reaction Steps
To a solution of 4-(1-benzyl-piperidin-4-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (1.51 g) in 20 mL acetic acid was added 0.23 g 10% palladium on carbon, the resulting suspension was shaken under hydrogen (50 psi) in Parr shaker apparatus for 12 hours. The suspension was filtered through a layer of celite and the solvent was removed under vacuum. To the residue was added 10% aq. NaOH and extracted with dichloromethane (2×). The combined organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. The title compound was obtained as clear syrup (1.16 g). ESI MS m/z 284 (M+H+); 1H NMR (400 MHz, CDCl3) δ 4.00 (m, 2H), 3.06 (d, J=10.1 Hz, 2H), 2.74 (m, 4H), 2.57 (t, J=10.1 Hz, 2H), 1.81 (t, J=14.1 Hz, 1H), 1.42 (s, 9H), 1.17 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884099B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-8cb274644af746f49ac8baca5975e425 |
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| Source note | uspto-grants-2011_02 |
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