HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235307Generated: October 30, 2026
Hydroxyamine hydrochloride → HCID 178518637, compound
https://huagongshe.com/reaction/235307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 6,7-dichloro-3-aminoquinoxalin-2(1H)-one | HCID 12773124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178518637 | HCID 178518637 | 79% |
Reaction Steps
An adaptation of the method of Harsanyi et al., Liebigs Ann. Chem. 190 (1973), was used. A mixture of 6,7-dichloro-3-aminoquinoxalin-2(1H)-one (50 mg, 0.22 mmol) and hydroxylamine hydrochloride (33 mg, 0.47 mmol; Aldrich Co.) in 2 mL of ethanol was heated to reflux. The resulting brown suspension was stirred under reflux for 12 h. The resulting brown suspension was allowed to cool to 25° C. A brown precipitate appeared. The mixture was vacuum filtered and the brown solid was washed with EtOH (5×2 mL) and dried in vacuum at 60° C. overnight to yield 42 mg (79%) of 6,7-dichloro-3-(hydroxyimino)-1,4-dihydroquinoxalin-2-one: mp dec.>270° C. 1H NMR (300 MHz, DMSO-d6) δ 11.306 (br s, 1H, NH), 11.049 (br s, 1H, NH), 10.148 (br s, 1H, NOH), 7.403 (s, 1H, H-5), 7.018 (s, 1H, H-8). Mass: calcd. for C8H5Cl2N3O2 (M+) M/Z 244.9759, found 244.9769.
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-379bbba0b6a146768d167268bc48a2d0 |
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| Source note | uspto-grants-1997_01 |
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