HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2-Amino-5-nitropyridin-3-yl)-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 5-Nitropyridine-2,3-diamine | HCID 3480151 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2-Amino-5-nitropyridin-3-yl)-4-nitrobenzamide | HCID 58932933 | 81% |
Reaction Steps
To a solution of 2,3-Diamino-5-nitropyridine (3) in dry pyridine (85 mL) was added 4-nitrobenzoylchloride (0.875 g, 4.7 mmol) and the mixture was stirred at room temperature for 20 h. The mixture was then poured into H2O (250 mL) and stirred for 30 minutes. The resulting yellow solid was collected by filtration and rinsed with H2O until no pyridine remained. The solid was dried in vacuuo at 80 C to give 6 as a yellow solid (1.15 g, 3.8 mmol, 81%). 1H NMR (500 MHz, DMSO-d6) δ10.12 (br s, 1H), 8.83 (d, J=2.55 Hz, 1H), 8.84 (d, J=8.5 Hz, 2H), 8.35 (d, J=2.45 Hz, 2H), 8.24 (d, J=8.7 Hz, 2H), 7.62 (br s, 2H). EIMS M−1 302.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256287B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-54fd63118593484c84c0b78d66da8d5d |
| Source note | uspto-grants-2007_08 |