HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055032Generated: October 29, 2026
Ammonium Hydroxide → 2-Bromo-6-chloro-3-methylquinoxaline
https://huagongshe.com/reaction/1055032
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | 6-chloro-3-methyl-1H-quinoxalin-2-one;7-chloro-3-methyl-1H-quinoxalin-2-one | HCID 131736342 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-6-chloro-3-methylquinoxaline | HCID 90016870 | 20.1% |
| Product | 3-Bromo-6-chloro-2-methylquinoxaline | HCID 90016962 | — |
Reaction Steps
6-Chloro-3-methylquinoxalin-2(1H)-one compound with 7-chloro-3-methylquinoxalin-2(1H)-one (300 mg, 771 μmol, Eq: 1.00) was stirred neat in phosphoryl tribromide (1.6 g, 5.58 mmol, Eq: 7.24). N,N-Dimethylformamide (1 drop) (771 μmol, Eq: 1.00) was added and the mixture was stirred at 105° C. for 1.5 h. The mixture was added to ice water and neutralized with aqueous 25% ammonium hydroxide. The precipitated solid was filtered and dried under high vacuum followed by preparative HPLC to give 3-Bromo-6-chloro-2-methyl-quinoxaline with 2-bromo-6-chloro-3-methyl-quinoxaline (40 mg, 10.1%) as a light brown solid. MS: m/z=195.03 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394311B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-5f73643ee45448a4b3cc6f2054ed1ae8 |
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| Source note | uspto-grants-2016_07 |
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