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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261050Generated: November 2, 2026

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

https://huagongshe.com/reaction/2261050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(3R,4R)-1-tert-butyl 3-ethyl 4-((R)-1-phenylethylamino)-piperidine-1,3-dicarboxylateHCID 11080151—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(3R,4R)-1-tert-butyl 3-ethyl 4-aminopiperidine-1,3-dicarboxylateHCID 5874561496.2%

Reaction Steps

A solution of 252D (1.18 g, 3.13 mmol) in MeOH (31 mL) was treated with ammonium formate (1.58 g, 25.1 mmol) and 10% Pd/C. The reaction mixture was heated to reflux for 14 hours then cooled to room temperature. The resulting solid was removed by filtration and washed with MeOH. The filtrate was dried (Na2SO4) and concentrated under reduced pressure to give 0.82 g (yield: 96%) of Compound 252E as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846931B2
Source datasetuspto-grants-2010_12
ORD IDord-64e6d431a32149cd8cd8a06899f9b3d9
Source noteuspto-grants-2010_12