HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595906Generated: October 30, 2026
N-bromobutanimide → 5-(5-Amino-6-bromopyrazin-2-yl)piperidin-2-one
https://huagongshe.com/reaction/595906
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-(5-Aminopyrazin-2-yl)piperidin-2-one | HCID 118045916 | — |
| Product | 5-(5-Amino-6-bromopyrazin-2-yl)piperidin-2-one | HCID 118045843 | — |
Reaction Steps
To 5-(5-aminopyrazin-2-yl)piperidin-2-one (25 mg, 0.13 mmol) acetonitrile (10 mL) solution at 0° C. was added NBS (23.2 mg, 0.13 mmol) and the reaction mixture was stirred at 0° C. for 30 min, then at room temperature for 4 h. The reaction mixture was concentrated, and the residue was basified by 1 N NaOH (140 ul), diluted with methanol (2 mL), concentrated. The residue was triturated with EtOAc (3×1 mL), and the EtOAc supernatants were collected, combined and concentrated and a light solid was obtained as crude 5-(5-amino-6-bromopyrazin-2-yl)piperidin-2-one which was used in next step without further purification. LCMS (m/z): 241/243 (MH+), 0.41 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-003c63f7b1924d64b9fdf63881a75a68 |
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| Source note | uspto-grants-2016_01 |
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