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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347727Generated: October 25, 2026

Triethylamine → 2-(4-ethoxycarbonyl-1-piperidinyl)-4-nitropyridine N-oxide

https://huagongshe.com/reaction/347727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant2-Bromo-4-nitropyridine N-oxideHCID 3904026—
SolventEthanolHCID 702—
Product2-(4-ethoxycarbonyl-1-piperidinyl)-4-nitropyridine N-oxideHCID 58801116111.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-bromo-4-nitropyridine N-oxide (12 g), which is prepared according to the method disclosed in J. Org. Chem., 21, 1077 (1956), in ethanol (300 ml) are added 4-piperidinecarboxylic acid ethyl ester (22 g) and triethylamine (11.6 ml), and the mixture is stirred at 80° C. for 5 hours. The reaction solution is concentrated under reduced pressure, and the residue is dissolved in ethyl acetate, washed with water, and the solvent is evaporated under reduced pressure to give the title compound (18 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176199B2
Source datasetuspto-grants-2007_02
ORD IDord-b2122ce626dd47209bab860b2c95742e
Source noteuspto-grants-2007_02