Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 6,7-Difluoro-5-nitro-1,4-dihydro-2,3-quinoxalinedione | HCID 10800253 | — |
| Catalyst | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10514172 | HCID 10514172 | 76% |
Reaction Steps
To a solution of 20 mg (0.082 mmol) of 6,7-difluoro-5-nitro-1,4-dihydroquinoxaline-2,3-dione in 0.5 mL of DMSO-d6 was added 2 drops of 30% ammonium hydroxide and the solution was heated at 80° C. for 24 h. To the mixture was added one more drop of 30% ammonium hydroxide and it was heated at 80° C. for 10 h. The mixture was added to 4 mL of water and then acidified with 2N HCl to pH=1. The precipitate was filtered, washed with water, and dried to leave a yellow solid (15 mg, 76%); mp 250° C. (dec.); 1H NMR (DMSO-d6), 7.202 (1, d, J=11.5), 7.232 (sb, 2), 11.15 (mb, 1), 12.0 (mb, 1). 19F NMR, -133.84 (d, J=11.6). MS, 240 (M+, 100), 212 (10), 177 (10), 166 (20). HRMS, Calcd for C8H5FN4O4 240.0290, found 240.0294.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631373 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-a5ae1c95958b469682aaea64e7a91558 |
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| Source note | uspto-grants-1997_05 |
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