Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 178514477 | HCID 178514477 | — |
| Product | HCID 178514504 | HCID 178514504 | — |
Reaction Steps
15 ml 89% nitric acid was ice-cooled and then gradually added 1 g (4,2 mmol) 6-azido-7-chloro-2,3-dihydroxyquinoxaline. After stirring at 0° C. for 15 min, the reaction mixture was poured into 100 ml ice-water. The crude product was recrystallized (acetone-methanol-water) to give 0,95 g (80%) 6-azido-7-chloro-2,3-dihydroxy-5-nitroquinooxaline. IR (KBr): 2450 cm-1 (N3). NMR (DMSO-d6) 12.3 (2H, broad s), 7.07 (1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057516 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-4cf201a4ffc74e3ba0342e324ca48ef1 |
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| Source note | uspto-grants-1991_10 |
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