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HRID 617285作成日:2026年10月25日

Sodium hydride → (S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazine

https://huagongshe.com/reaction/617285

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物ChloropyrazineHCID 73277—
反応物(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazineHCID 4432587297%

反応手順

(S)-(-)-1-Methyl-2-pyrrolidinemethanol (Aldrich Chemical Co., 0.5 g, 4.34 mmol) was dissolved in anhydrous THF and brought to 0° C. NaH ((80% dispersion in mineral oil), 131 g, 4.56 mmol) was added and the reaction mixture was allowed to warm to room temperature with stirring. After 30 minutes 2-chloropyrazine (0.497 g, 4.34 mmol) was added via syringe. The mixture was stirred for 48 hours. The solvent was then evaporated in vacuo and the mixture diluted with chloroform, washed with saturated NaHCO3 and a brine solution. The organic layer was then dried over MgSO4. The resulting crude material was purified by flash chromatography (10% MeOH/CHCl3) to give 0.81 g (97% yield) of the title compound as an oil. TLC Rf =0.3 (10% MeOH/CHCl3). MS (DCI/NH3) m/e 194 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ: 8.24 (d, J=1.5 Hz, 1H, 8.11 (d, J=3 Hz, 1H), 8.07 (dd, J=3, 1.5 Hz, 1H), 4.36 (dd, J=9, 6 Hz, 1H), 4.28 (dd, J=9, 6 Hz, 1H), 3.16-3.08 (m, 1H, 2.7-2.58 (m, 1H, 2.47 (s, 3H), 2.34-2.24 (m, 1H, 2.08-1.93 (m, 1H, 1.91-1.67 (m, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05948793
出典データセットuspto-grants-1999_09
ORD IDord-bce61a14f88c4b30ac79a275727ce2e8
出典メモuspto-grants-1999_09