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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602454Generated: November 3, 2026

tert-Butyl cis-5-azido-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidine-1-carboxylate → tert-Butyl cis-5-amino-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/602454

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl cis-5-azido-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidine-1-carboxylateHCID 86624147—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl cis-5-amino-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidine-1-carboxylateHCID 67269815—

Reaction Steps

The mixture of tert-butyl cis-5-azido-2-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidine-1-carboxylate (253 mg, 0.743 mmol, step 4 of Example 2) and 10 wt. % palladium on carbon (50 mg) in methanol (5 mL) was stirred under hydrogen (4 atom) at room temperature for 7 h. The mixture was filtered through a pad of Celite washing with methanol and the filtrate was concentrated to give 244 mg (quant.) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906532B2
Source datasetuspto-grants-2011_03
ORD IDord-dd86276b187b4f44b877a4eef48252ff
Source noteuspto-grants-2011_03