HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772587Generated: November 2, 2026
N-bromobutanimide → (5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)methanol
https://huagongshe.com/reaction/1772587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (8-Morpholinoimidazo[1,2-a]pyrazin-2-yl)methanol | HCID 117728187 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)methanol | HCID 117727888 | 45.9% |
Reaction Steps
To a solution of compound 1d (2.40 g, 10.3 mmol) in ACN (200 mL) was added NBS (2.40 g, 13.5 mmol) in portions at −20° C. The resulting solution was stirred at −20° C. for 2 h, and was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with EtOAc/petroleum ether (1:1 v/v) to obtain compound 1e as a yellow solid (1.48 g, 41% yield). Mass Spectrum (LCMS, ESI pos.): Calcd. for C11H13BrN4O2: 313.0 (M+H). Found 313.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249163B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-2d02f32f55504872bc963e8ffeceb846 |
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| Source note | uspto-grants-2016_02 |
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