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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420520Generated: October 25, 2026

Chloropyrazine → (S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazine

https://huagongshe.com/reaction/1420520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloropyrazineHCID 73277—
Reactant(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazineHCID 44325872—

Reaction Steps

A solution of (S)-1-methyl-2-pyrrolidinemethanol (1.15 g) in THF (45 mL) was treated with potassium tert-butoxide (1.2 g). After 10 min, chloropyrazine was added and the reaction stirred for 1.5 h. The reaction was quenched with 5 N HCl (4 mL) and the solvent evaporated. The residue was suspended in water and extracted with ether. The aqueous fraction was made basic and extracted with CHCl3. The extracts were dried, the solvent evaporated, and the residue purified by radial chromatography eluting with 20%-EtOH-2%-NH4OH-CHCl3 to give (S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazine (1.1). The HCl salt crystallized from EtOAc as a white solid, m.p. 121-122° C. (Compound 28)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071900
Source datasetuspto-grants-2000_06
ORD IDord-51486aa179df4d81a5ebefb9c6f90d78
Source noteuspto-grants-2000_06