HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439473Generated: October 30, 2026
Stannous Chloride → 5-Amino-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione
https://huagongshe.com/reaction/439473
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Acea-1031 | HCID 9799201 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione | HCID 10520762 | 64.7% |
Reaction Steps
To a stirred mixture of 5-nitro-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione (327 mg, 0.89 mMol) in ethanol (10 mL) was added SnCl2 ·2H2O (1.0 g, 4.45 mMol) in one portion. The mixture was refluxed at 80° C. (oil bath 90° C.) with stirring for 4 h. The mixture was then cooled to room temperature and the yellow precipitate was collected by filtration, followed by washing with cold ethanol (2×1 mL), to get 227 mg (76%) of crude title product (contains minor impurities by NMR). Crystallization from DMSO/H2O gave 193 mg of pure title product as bright yellow needles; mp: 324°-6° C. (dec.), changed color from 270° C. IR (KBr, cm-1): 3456; 3281; 1700; 1643. NMR (1H, DMSO-d6): δ5.844 (s, 2H); 6.732 (s, 1H); 11.257 (s, 1H); 11.810 (s, 1H). Purity:>96.96% by HPLC. HRMS: calcd for C8H5N3O2Br2 (M+) m/z 332.8747; found: 332.8754. Potency relative to DCK: 341%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514680 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-31f99e8f432f4326880597a862dff916 |
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| Source note | uspto-grants-1996_05 |
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