HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-3,5-dinitropyridine → 5-Nitropyridine-2,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-3,5-dinitropyridine | HCID 504340 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Nitropyridine-2,3-diamine | HCID 3480151 | 80.6% |
Reaction Steps
To a suspension of 61 (1.617 g, 8.79 mmol) in MeOH (75 mL) was added 20% aq. (NH4)2S (15 mL, 44 mmol) dropwise at room temperature with stirring. The resulting dark-red solution was stirred at room temperature for 0.5 h, then refluxed for 0.5 h, then cooled to room temperature. The resulting mixture was filtered. The filtrate was concentrated to about 30 mL and cooled in ice-water. The precipitate was filtered, washed with cooled EtOH (2×5 mL), and dried to give 1.092 g (80%) of 62 as a deep red powder, mp 260°-2° C.(dec) (Lit., 260° C., Chemical Abstracts 65:3826 (1966)). 1H NMR (DMSO-d6): 5.311 (s, 2H), 6.984 (s, 2H), 7.342(d, 1H, J=2.2), 8.171 (d, 1H, J=2.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620978 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-d6ab1776ad7141ce84103b351203c2d5 |
| Source note | uspto-grants-1997_04 |