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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615397Generated: October 30, 2026

HCID 71073872, compound → HCID 66691782, compound

https://huagongshe.com/reaction/1615397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71073872HCID 71073872—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66691782HCID 66691782—

Reaction Steps

The N-(4-(2-(1,2,3-triazol-1-yl)-ethyl)-phenyl)-4-benzyloxycarbonylaminopiperidine (1.3 g, 50 mmol) obtained in Example 7 (6) was dissolved in methanol (13 ml) and THF (13 ml), and 10% palladium-carbon (hereinafter referred to as Pd—C) (130 mg) was added, followed by stirring at room temperature in an atmosphere of hydrogen gas for 24 hours. After the insoluble material was filtered with Celite, the solvent was evaporated from the filtrate under reduced pressure, thereby obtaining N-(4-(2-(1,2,3-triazol-1-yl)-ethyl)-phenyl)-4-aminopiperidine (870 mg, 99%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765750B2
Source datasetuspto-grants-2014_07
ORD IDord-2f8300cfc4374f619311afa3aae3fdec
Source noteuspto-grants-2014_07