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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409924Generated: October 31, 2026

HCID 71233371, compound → HCID 71233145, compound

https://huagongshe.com/reaction/2409924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71233371HCID 71233371—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 71233145HCID 7123314586%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815909B2
Source datasetuspto-grants-2014_08
ORD IDord-eda928b29deb47ffa4c8115968523ec6
Source noteuspto-grants-2014_08