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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminopyrazineHCID 78747—
Reactant1-tert-Butyl 2-methyl (2S)-2-methylpyrrolidine-1,2-dicarboxylateHCID 59436426—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-Methyl-N-(pyrazin-2-yl)pyrrolidine-2-carboxamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415340B2
Source datasetuspto-grants-2013_04
ORD IDord-53ccca1c357e4b07a2af256d5f13d079
Source noteuspto-grants-2013_04