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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402075Generated: October 30, 2026

(+/-)-cis-4-Azidomethyl-3-fluoro-piperidine-1-carboxylic acid tert-butyl ester → tert-butyl (3S,4R)-4-(aminomethyl)-3-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/402075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-cis-4-Azidomethyl-3-fluoro-piperidine-1-carboxylic acid tert-butyl esterHCID 86657835—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl (3S,4R)-4-(aminomethyl)-3-fluoropiperidine-1-carboxylateHCID 86657837—

Reaction Steps

To a stirred solution of (±)-cis-4-azidomethyl-3-fluoro-piperidine-1-carboxylic acid tert-butyl ester (0.68 mmol, 160 mg) in methanol (1.5 mL) was added Pd—C (20% by wt., 35 mg). The reaction was hydrogenated under balloon pressure for 2 h at room temperature. The reaction was filtered through a bed of celite. The solvent was evaporated to provide (±)-cis-4-aminomethyl-3-fluoro-piperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741900B2
Source datasetuspto-grants-2014_06
ORD IDord-8232a758eb144d3cbff3d564b46df2fd
Source noteuspto-grants-2014_06