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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890439Generated: October 30, 2026

Potassium Carbonate → 4-(6-Methoxy-3-nitro-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1890439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant2-Chloro-6-methoxy-3-nitropyridineHCID 2795029—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product4-(6-Methoxy-3-nitro-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 67130835—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-amino-1-Boc-piperidine (commercial; 6.7 g, 35 mmol), 2-chloro-6-methoxy-3-nitro-pyridine (1 eq.) and K2CO3 (1 eq.) in MeCN (100 mL) and DMF (30 mL) was heated at 60° C. for 3 h. The mixture was filtered and concentrated in vacuo. The residue was taken up in ether/water 1:1, the org. phase dried over MgSO4 and concentrated. The residue was triturated with EA and filtered to afford 4.5 g of pure product. The filtrate was concentrated and purified by CC (Hept/EA 9:1, 4:1, 2:1) to give another 4 g of product. In total 8.5 g (70% yield) of a yellow solid were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507478B2
Source datasetuspto-grants-2013_08
ORD IDord-d46bb63cb7c34534852b299b8e0f1466
Source noteuspto-grants-2013_08