Potassium Nitrate → 5-Chloro-6-nitro-7-fluoro-1,4-dihydro-2,3-quinoxalinedione

HRID 53744Notes

Reaction equation

[Cl:1][C:2]1[CH:11]=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[NH:4][C:5](=[O:14])[C:6](=[O:13])[NH:7]2.[N+:15]([O-])([O-:17])=[O:16].[K+]>OS(O)(=O)=O>[Cl:1][C:2]1[C:11]([N+:15]([O-:17])=[O:16])=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[NH:4][C:5](=[O:14])[C:6](=[O:13])[NH:7]2

Participants

Conditions

Temperature: 0 °C

Procedure

The Method of Cheeseman, supra. was adapted. 5-Chloro-7-fluoro-1,4-dihydro-2,3-quinoxalinedione (30 mg, 0.14 mMol) was dissolved in concentrated H2SO4 (0.5 ml) at 0° C. for 30 min, and KNO3 (17 mg, 0.17 mmole, Baker) was added in one portion to this solution. The mixture was stirred at 0° C. for 3 h, then at room temperature for 30 h. It was poured into ice water (5 g) and the precipitate was collected by filtration. The precipitate was dissolved in 1N NaOH (5 mL), then was acidified to pH=2 with 4N HCl to give a cream precipitate, which was collected by filtration, then was dried in the air at 50° C. for 4 h, affording the pure (by NMR) title compound 5-chloro-6-nitro-7-fluoro-1,4-dihydro-2,3-quinoxalinedione (31 mg, 85.4%), as a white amorphous solid. mp: decomposed from 280° C. IR (KBr, cm-1): 3600, 3462, 3131, 1712, 1612, 1550. NMR (1H, DMSO-d6): δ 7.106 (d, J=10.2 Hz, 1H), 11.800 (s, 1H), 12.371 (s. 1H). HRMS: calcd. for C8H3N3O4ClF (M+) m/z: 258.9795, found: 258.9790.

Workup

waitat room temperature for 30 h
filtrationthe precipitate was collected by filtration
dissolutionThe precipitate was dissolved in 1N NaOH (5 mL)
customto give a cream precipitate, which
filtrationwas collected by filtration
customwas dried in the air at 50° C. for 4 h

Sources & evidence

ORD record: ord-87c3eed2fd7841729086f8a1b6d7b5cd
Source dataset: uspto-grants-1997_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05620979

Reaction notes

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