HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409924Generated: October 31, 2026
HCID 71233371, compound → HCID 71233145, compound
https://huagongshe.com/reaction/2409924
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 71233371 | HCID 71233371 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71233145 | HCID 71233145 | 86% |
Reaction Steps
10% Pd/C (0.20 gm, 0.19 mmol) was added to a solution of benzyl 3-((1R,2R)-2-(tert-butoxycarbonylamino)cyclohexylamino)piperidine-1-carboxylate, (1.73 gm, 4.01 mmol) in MeOH (14.6 mL) and AcOH (1.46 mL). A H2 atmosphere was then introduced via balloon. After 1 h the reaction mixture was filtered through Celite. The catalyst was rinsed with MeOH and the filtrate was concentrated. The residue was partitioned between EtOAc and sat. NaHCO3. The aqueous phase was isolated and extracted with EtOAc. All organic phases were combined, washed with saturated aqueous NaCl, dried over MgSO4, filtered and concentrated to give the product tert-butyl (1R,2R)-2-(piperidin-3-ylamino)cyclohexylcarbamate (1.02 gm, 3.43 mmol, 86% yield) as a white foam. Anal. Calcd. for C16H31N3O2 m/z 297.2, found: 298.2 (M+H)+. Crude product was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815909B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-eda928b29deb47ffa4c8115968523ec6 |
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| Source note | uspto-grants-2014_08 |
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