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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593468Generated: October 31, 2026

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

https://huagongshe.com/reaction/1593468

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 numberUS07297695B2
Source datasetuspto-grants-2007_11
ORD IDord-080a6bbcc21c46389f8dbc61b8d99ce3
Source noteuspto-grants-2007_11