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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993669Generated: October 30, 2026

Sodium Carbonate → tert-Butyl 4-(5-nitropyridine-2-ylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1993669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventEthanolHCID 702—
Producttert-Butyl 4-(5-nitropyridine-2-ylamino)piperidine-1-carboxylateHCID 53255493—

Reaction Steps

Dissolve N-Boc-4-aminopiperidine (0.9 g, 4.8 mmol) in dry ethanol and add solid sodium carbonate (0.8 g, 7.9 mmol) at 0° C., followed by 2-chloro-5-nitro-pyridine (0.6 g, 3.9 mmol). Stir the solution at room temperature overnight, then heat the solution at 9° C. for 6 hours. Stir at room temperature overnight. Evaporate the solvent under reduced pressure and partition the crude mixture between EtOH and water. Extract with EtOAc and wash the organic layer with saturated aq. sodium chloride solution. Combine organic layers and dry over MgSO4. Filter and evaporate the solvent in order to obtain 4-(5-Nitro-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652015B2
Source datasetuspto-grants-2010_01
ORD IDord-5889c8e2a7d948fdb556c226a1f8094e
Source noteuspto-grants-2010_01