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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362833Generated: October 29, 2026

HCID 59898559, compound → HCID 59898565, compound

https://huagongshe.com/reaction/1362833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59898559HCID 59898559—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 59898565HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884099B2
Source datasetuspto-grants-2011_02
ORD IDord-8cb274644af746f49ac8baca5975e425
Source noteuspto-grants-2011_02