HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595881Generated: November 1, 2026
N-bromobutanimide → 2-(5-Amino-6-bromopyrazin-2-yl)ethanol
https://huagongshe.com/reaction/595881
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(5-Aminopyrazin-2-yl)ethanol | HCID 118045507 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(5-Amino-6-bromopyrazin-2-yl)ethanol | HCID 118046118 | — |
Reaction Steps
To a solution of 2-(5-aminopyrazin-2-yl)ethanol (30 mg, 0.216 mmol) in CH3CN (719 μL) was added NBS (38.4 mg, 0.216 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 30 min. The reaction mixture was quenched by sat. NaHCO3, then extracted by EtOAc, The combined organic layer was washed with water and brine, dried over anhydrous sodium sulfate. Filtered and concentrated in vacuo yielding crude 2-(5-amino-6-bromopyrazin-2-yl)ethanol which was used in next step reaction without purification. LCMS (m/z): 218.0/220.0 (MH+), 0.33 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-8a4574e641db47e891c13ebf93686b17 |
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| Source note | uspto-grants-2016_01 |
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