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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | 2-Bromo-4-nitropyridine N-oxide | HCID 3904026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-ethoxycarbonyl-1-piperidinyl)-4-nitropyridine N-oxide | HCID 58801116 | 111.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176199B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-b2122ce626dd47209bab860b2c95742e |
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| Source note | uspto-grants-2007_02 |
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