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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178515551 | HCID 178515551 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,8-Dibenzyl-3-methoxy-6-phenyl-imidazo[1,2-a]pyrazine | HCID 66702735 | 82.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08106052B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-0f0825bd648f482e87e4e0e915de9b43 |
|---|
| Source note | uspto-grants-2012_01 |
|---|