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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744406Generated: November 1, 2026

Ammonia → 2-Nitropyridine

https://huagongshe.com/reaction/1744406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-PyridoneHCID 8871—
Reactant1-Methyl-3,5-dinitro-1H-pyridin-2-oneHCID 3621236—
Product2-NitropyridineHCID 26998—

Reaction Steps

In addition, compounds referred to hereinbelow as 7e and 7f were synthesized by modifying the method described by Tohda et al, Nucleophilic Reaction upon Electron-Deficient Pyridone Derivatives X. One-Pot Synthesis of 3-Nitropyridines by Ring Transformation of 1-Methyl-3,5-dinitro-2-pyridone with Ketones or Aldehydes in the Presence of Ammonia, Bull. Chem. Soc. Jpn. 1990, 63, 2820–2827, for producing nitropyridine by using 3,5 dinitro-1-methyl-2-pyridone which produced the nitro compound 7e which was reduced to the amine 7f.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015326B1
Source datasetuspto-grants-2006_03
ORD IDord-52e0d0435e6f4e4090133eb4938ddb76
Source noteuspto-grants-2006_03