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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412295Generated: October 29, 2026

HCID 22258787, compound → HCID 135550591, compound

https://huagongshe.com/reaction/412295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22258787HCID 22258787—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 135550591HCID 135550591—

Reaction Steps

A solution of tert-butyl 3-{2-amino-3-(azidomethyl)-6-[2-(benzyloxy)phenyl]-4-pyridinyl}-1-piperidinecarboxylate (0.030 g, 0.058 mmol) in ethyl acetate (1.0 mL) was hydrogenated at 1 atm in the presence of palladium on charcoal (10%, 0.015 g) overnight. The resulting mixture was filtered and washed with ethyl acetate. The combined filtrate was concentrated under reduced pressure to give tert-butyl 3-[2-amino-3-(aminomethyl)-6-(2-hydroxyphenyl)-4-pyridinyl]-1-piperidinecarboxylate, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562811B1
Source datasetuspto-grants-2003_05
ORD IDord-048959430a9a4c0b962c9fc30359bf55
Source noteuspto-grants-2003_05