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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723478Generated: October 30, 2026

Ammonium formate → 1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/723478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(3S,4R)-1-tert-butyl 3-ethyl 4-((R)-1-phenylethylamino)-piperidine-1,3-dicarboxylateHCID 66952586—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylateHCID 5874549496%

Reaction Steps

A solution of 252C (2.6 g, 6.9 mmol) in EtOH (100 mL) was treated with ammonium formate (3.5 g, 55.3 mmol) and 10% Pd/C (390 mg). The reaction mixture was heated to reflux under a nitrogen atmosphere for three hours. The resulting suspension was filtered through a pad of celite and concentrated in vacuo to afford 1.8 g (yield: 96%) Compound 259A as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141571B2
Source datasetuspto-grants-2006_11
ORD IDord-e81da44e67994ff0b1f11b26b4e7da9a
Source noteuspto-grants-2006_11