HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270331Generated: October 25, 2026
Hydrogen Bromide → [4-(5-Bromo-6-ethyl-3-methoxypyrazin-2-yl)-3-methoxyphenoxy]trifluoromethane
https://huagongshe.com/reaction/1270331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 3-Ethyl-6-methoxy-5-[2-methoxy4-(trifluoromethoxy)phenyl]pyrazin-2-ylamine | HCID 22248898 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Water | HCID 962 | — |
| Product | [4-(5-Bromo-6-ethyl-3-methoxypyrazin-2-yl)-3-methoxyphenoxy]trifluoromethane | HCID 22248930 | — |
Reaction Steps
To a stirred solution of 3-ethyl-6-methoxy-5-[2-methoxy-4-(trifluoromethoxy)phenyl]pyrazin-2-ylamine (86 mg, 0.25 mmol) in 48% hydrogen bromide (0.3 mL) at 0° C. is added a solution of sodium nitrite (21 mg, 0.3 mmol) in water (1 mL). After 1.5 h copper bromide (43 mg, 0.3 mmol) is added and the mixture heated to 70° C. for 1 h. The mixture is cooled to room temperature and extracted with ether. The extracts are dried (sodium sulfate), filtered and concentrated to give [4-(5-bromo-6-ethyl-3-methoxypyrazin-2-yl)-3-methoxyphenoxy]trifluoromethane (76 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202250B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-16930d0620f742358c61ef5412fec4bc |
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| Source note | uspto-grants-2007_04 |
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