HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487922Generated: October 25, 2026
Sodium hydride → 1-(2-Methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine
https://huagongshe.com/reaction/487922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Nitromethylene)imidazolidine | HCID 3014763 | — |
| Reactant | 2-(Chloromethyl)-5-methylpyrazine | HCID 13221025 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine | HCID 184600 | 23% |
Reaction Steps
2-Nitromethyleneimidazolidine (12.9 g) was dissolved in dry dimethylformamide (100 ml), and at room temperature 60% oily sodium hydride (4.4 g) was added. The mixture was stirred at room temperature until the generation of hydrogen ceased. Then 2-methyl-5-pyrazinylmethyl chloride (14.3 g) was added at room temperature, and the mixture was stirred at 40° C. for 8 hours. After cooling to room temperature, the reaction mixture was added to 200 ml of water, and extracted with dichloromethane. On distilling off dichloromethane from the organic layer under reduced pressure, 1-(2-methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine (5.4 g) was obtained as yellow crystals having a melting point of 163° to 166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298507 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-3b8a034d74b74f97a1cfd4ab80ec6caa |
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| Source note | uspto-grants-1994_03 |
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