HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961379Generated: October 26, 2026
Aminopyrazine → (S)-2-Methyl-N-(pyrazin-2-yl)pyrrolidine-2-carboxamide
https://huagongshe.com/reaction/1961379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | 1-tert-Butyl 2-methyl (2S)-2-methylpyrrolidine-1,2-dicarboxylate | HCID 59436426 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-Methyl-N-(pyrazin-2-yl)pyrrolidine-2-carboxamide | HCID 59436345 | — |
Reaction Steps
To a stirred solution of pyrazin-2-amine (1.56 g, 16.44 mmol) in THF (30 ml) was added isopropyl magnesium chloride (7.8 ml, 15.62 mmol) (2.0 M THF solution) dropwise at 0° C. under nitrogen. The resulting suspension was stirred at RT for 30 min. A solution of (S)-1-tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate (1.0 g, 4.11 mmol) solid was added to the reaction mixture. The reaction mixture was stirred at RT for 6 h, quenched with MeOH, and concentrated. The residue was dissolved in EtOAc (120 ml) and washed with 1N HCl to remove the excess pyrazin-2-amine, water, and brine, dried over Na2SO4. The crude product was dissolved in methanol and 4N HCl in dioxane (4 mL) was added. The reaction mixture was stirred at room temperature overnight and the crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415340B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-53ccca1c357e4b07a2af256d5f13d079 |
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| Source note | uspto-grants-2013_04 |
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