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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419730Generated: October 26, 2026

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

https://huagongshe.com/reaction/1419730

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 5N 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 numberUS05888999
Source datasetuspto-grants-1999_03
ORD IDord-1a7d87a4e36747519e6ca2c194ea09a4
Source noteuspto-grants-1999_03