Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503358Generated: October 25, 2026

N-Iodosuccinimide → 6-Bromo-3-iodo-8-(methylthio)imidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/1503358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant6-Bromo-8-(methylthio)imidazo[1,2-A]pyrazineHCID 53249869—
SolventDimethylformamideHCID 6228—
Product6-Bromo-3-iodo-8-(methylthio)imidazo[1,2-a]pyrazineHCID 5759960980.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 6-bromo-8-methylsulfanyl-imidazo[1,2-a]pyrazine (210.0 g, 860.3 mmol) in DMF (4200 mL) was added NIS (212.9 g, 946.3 mmol, 1.1 eq) in one portion at rt. After 18 h stirring at 60° C. the dark solution was evaporated and the brown residue was dissolved in DCM (7 L), washed with water (2×5 L) and sole (2×5 L) and dried over sodium sulphate. Crystallization by careful removal of solvent yielded 255 g (80.1%) 6-bromo-3-iodo-8-methylsulfanyl-imidazo[1,2-a]pyrazine: 1H-NMR (300 MHz, d6-DMSO): δ=8.24 (1H, s), 7.79 (1H, s), 2.46 (3H, s) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212184B2
Source datasetuspto-grants-2015_12
ORD IDord-fa88b69c3c3048ccb341051ab2f72c21
Source noteuspto-grants-2015_12