HuagongsheHuagongshe Chemistry Print Report · For research reference only
2(1H)-Quinoxalinone → HCID 15667664, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2(1H)-Quinoxalinone | HCID 14526 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 6-Nitroquinoxalin-2-one | HCID 1042919 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 15667664 | HCID 15667664 | — |
Reaction Steps
The procedure of Example I.D. was followed except the quinoxalin-2-one was converted to the 6-nitroquinoxalin-2-one by first dissolving in conc. H2SO4 and cooling in an ice bath, and adding KNO3 in 3 portions. The product was collected by conventional technique and subsequently converted to 2-hydrazino-6-nitroquinoxaline. This compound was reacted with triethylorthoformate as per Example I.D., yielding 7-nitro-1,2,4-triazolo[4,3-a]quinoxaline (16).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153196 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-761e282b1c9f48be85ab9368316d359b |
| Source note | uspto-grants-1992_10 |