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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1419730생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1419730

반응식

참여 물질

역할이름HCID투입량
반응물ChloropyrazineHCID 73277—
반응물(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazineHCID 44325872—

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05888999
출처 데이터셋uspto-grants-1999_03
ORD IDord-1a7d87a4e36747519e6ca2c194ea09a4
출처 메모uspto-grants-1999_03