Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772635Generated: November 4, 2026

Ethyl (5-bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)carbamate → 5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-amine

https://huagongshe.com/reaction/1772635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (5-bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)carbamateHCID 131734673—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product5-Bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-amineHCID 117728054—

Reaction Steps

A suspension of ethyl (5-bromo-8-morpholinoimidazo[1,2-a]pyrazin-2-yl)carbamate (1.2 g, as prepared above) in 5 N aqueous NaOH was heated at reflux for 18 h. The reaction mixture was allowed to cool to rt, diluted with water (50 mL) and extracted with DCM (3×50 mL). The combined DCM layers were dried over Na2SO4 and concentrated under reduced pressure to give compound 21b, which was dried under reduced pressure overnight and used in next step without further purification. Mass Spectrum (LCMS, ESI pos.) Calcd. For C10H12BrN5O: 298.0 (M+H). Found 298.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-4173e56ccfe8429fa5cf93d92bcd8799
Source noteuspto-grants-2016_02