Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809179Generated: November 1, 2026

Chloroacetone → 8-Chloro-2-methylimidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/1809179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-3-chloropyrazineHCID 276224—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product8-Chloro-2-methylimidazo[1,2-a]pyrazineHCID 133890827.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-amino-3-chloropyrazine (10 g, 77.5 mmol), chloroacetone (30 mL, 387 mmol) in MeOH (25 mL) is refluxed overnight at 88° C. It is then stirred for 1 h at 0° C. and any solid that forms, is filtered off and washed twice with MeOH (5 mL). The mother liq. are evaporated, diluted with EtOAc, and washed with HCl 2N, water and brine. The water and HCl mother liq. are evaporated to give a yellow solid that is neutralized with a saturated solution of K2CO3 in water, extracted with DCM, dried with MgSO4 anh. filtered and concentrated. The crude material is purified by column chromatography using a gradient of (DCM/MeOH: 1/0 to 99/1) to give 8-Chloro-2-methyl-imidazo[1,2-a]pyrazine as an orange solid (1.02 g, 7.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362018B2
Source datasetuspto-grants-2013_01
ORD IDord-11bc6c510268416392ca4501d243b67c
Source noteuspto-grants-2013_01