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HRID 1419730作成日:2026年10月27日

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

https://huagongshe.com/reaction/1419730

反応式

関与物質

役割名称HCID仕込み量
反応物ChloropyrazineHCID 73277—
反応物(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazineHCID 44325872—

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05888999
出典データセットuspto-grants-1999_03
ORD IDord-1a7d87a4e36747519e6ca2c194ea09a4
出典メモuspto-grants-1999_03