Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178473438 | HCID 178473438 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 178507818 | HCID 178507818 | 87% |
Reaction Steps
A mixture of 5 g (15,4 mmol) 7-chloro-6-ethoxycarbonylamino-5-nitro-2,3-dihydroxyquinoxaline and 10 g potassium hydroxide in 60 ml 2-methoxyethanol was refluxed for 15 min. After cooling to 25° C., the reaction mixture was added 20 ml 2-methoxyethanol and 40 ml ether. The precipitated black product was filtered off and washed with ether. The crude product was dissolved in 100 ml water. Addition of 4N hydrochloric acid to pH 5-6 gave 3,4 g (87%) 6-amino-7-chloro-5-nitro-2,3-dihydroxyquinoxaline as red crystals, m.p.>300° C. NMR (DMSO-d6) 12.3 (2H, broad m), 7.40 (1H,s), 6.8 (2H, broad s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075306 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-76b1a0bbb38045f1975e6fceaa70069f |
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| Source note | uspto-grants-1991_12 |
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