HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-Pyridone | HCID 8871 | — |
| Reactant | 1-Methyl-3,5-dinitro-1H-pyridin-2-one | HCID 3621236 | — |
| Product | 2-Nitropyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105675B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-ac6dfc606a904e0897f8a9972061a21b |
| Source note | uspto-grants-2006_09 |