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Chloropyrazine → (S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloropyrazine | HCID 73277 | — |
| 反応物 | (2S)-1-Methyl-2-pyrrolidinemethanol | HCID 643492 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazine | HCID 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 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)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06030966 |
| 出典データセット | uspto-grants-2000_02 |
| ORD ID | ord-a97500dcfe004e03807b7b74d83d48f4 |
| 出典メモ | uspto-grants-2000_02 |