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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 617285생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/617285

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물ChloropyrazineHCID 73277—
반응물(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-(1-methyl-2-pyrrolidinylmethoxy)pyrazineHCID 4432587297%

반응 단계

(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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05948793
출처 데이터셋uspto-grants-1999_09
ORD IDord-bce61a14f88c4b30ac79a275727ce2e8
출처 메모uspto-grants-1999_09