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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424457Generated: October 29, 2026

Methyl iodide → 2,8-Dibenzyl-3-methoxy-6-phenyl-imidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/424457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178515551HCID 178515551—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2,8-Dibenzyl-3-methoxy-6-phenyl-imidazo[1,2-a]pyrazineHCID 6670273582.2%

Reaction Steps

To a stirred solution of 2,8-dibenzyl-6-phenyl-7H-imidazo[1,2-a]pyrazin-3-one (0.25 g, 0.6 mmol) in dry DMF (10 mL) at ambient temperature under argon was added diisopropylethylamine (1.1 mL, 6.0 mmol) all at once, followed by dropwise addition of methyl iodide (0.4 mL, 6.0 mmol). After stirring for 1 h the reaction was complete by TLC analysis. The reaction mixture was diluted with dichloromethane (75 mL) and washed twice with water. The organic extracts were dried over anhydrous sodium sulfate, filtered and evaporated to provide a brown oil. The crude oil was purified by flash chromatography on silica gel (30 g) using dichloromethane as mobile phase. Appropriate fractions were pooled and evaporated to afford 200 mg (77%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106052B2
Source datasetuspto-grants-2012_01
ORD IDord-0f0825bd648f482e87e4e0e915de9b43
Source noteuspto-grants-2012_01