HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235299Generated: October 26, 2026
O-Phenylenediamine → 3-Aminoquinoxalin-2(1H)-one
https://huagongshe.com/reaction/235299
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 2-ethoxy-2-thioxoAcetamide | HCID 21613763 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Aminoquinoxalin-2(1H)-one | HCID 4738040 | 18% |
Reaction Steps
An adaptation of the method of Burrell et al., J. Chem. Soc. Perkin I. 2707 (1973), was used. A mixture of 1,2-phenylenediamine (324 mg, 3.00 mmol; Aldrich Co.) and ethyl thiooxamate (400 mg, 3.00 mmol; Aldrich Co.) in 7.5 mL of ethanol was heated to reflux. The resulting solution was stirred under reflux for 3 h. The resulting suspension was cool 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 85 mg (18%) of 3-aminoquinoxalin-2(1H)-one as a pale yellow solid (McKillop et al., Tetrahedron Lett. 23:3357 (1982)): mp dec.>320° C. 1H NMR (300 MHz, DMSO-d6) δ 7.261-7.075 (m, 4H, H-5+H-6+H-7+H-8). LRMS: 161 (M+, 100%), 133 (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-3d74b713e29c4316b19d0c96a0e2d235 |
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| Source note | uspto-grants-1997_01 |
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