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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(8-Morpholinoimidazo[1,2-a]pyrazin-2-yl)methanolHCID 117728187—
SolventAcetonitrileHCID 6342—
Product(5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)methanolHCID 11772788845.9%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-2d02f32f55504872bc963e8ffeceb846
Source noteuspto-grants-2016_02