HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235303Generated: October 27, 2026
3-Bromo-4,5-diaminobenzotrifluoride → HCID 23354368, compound
https://huagongshe.com/reaction/235303
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-4,5-diaminobenzotrifluoride | HCID 735785 | — |
| Reactant | 2-ethoxy-2-thioxoAcetamide | HCID 21613763 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 23354368 | HCID 23354368 | 27.1% |
Reaction Steps
An adaptation of the method of Burrell et al., J. Chem. Soc. Perkin I. 2707 (1973), was used. A mixture of 3-bromo-5-trifluoromethyl-1,2-phenylenediamine (384 mg, 1.50 mmol; Maybridge Co.) and ethyl thiooxamate (220 mg, 1.70 mmol; Aldrich Co.) in 4 mL of 1-butanol was heated to reflux. The resulting solution was stirred under reflux for 6 h. The resulting suspension was cooled to 25 ° C. A pale yellow precipitate appeared. The mixture was vacuum filtered and the solid was washed with EtOH (5×2 mL) and dried in vacuum at 60° C. overnight to yield 125 mg (27.1%) of 5-bromo-7-trifluoromethyl-3-aminoquinoxalin-2(1H)-one (tentatively named as this since the regiochemistry is not sure) as a pale yellow solid of a new compound: mp dec.>267° C. 1H NMR (300 MHz, DMSO-d6) δ 7.680 (s, 1H, H-7), 7.495 (s, 1H, H-5). LRMS: 307 (M+, 100%), 280 (50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597922 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-e141d4861532484682b95da0738327bd |
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| Source note | uspto-grants-1997_01 |
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