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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045생성일: 2026년 10월 24일

Sodium hydride → 5-Ethynyl-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine

https://huagongshe.com/ko/reaction/1045

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물5-(2-Hydroxy-2-methyl-3-butynyl)-3-(1-methyl-5-pyrrolidin-2-onyl)pyridineHCID 19694325—
반응물Toluene acetoneHCID 20247278—
용매TolueneHCID 1140—
생성물5-Ethynyl-3-(1-methyl-5-pyrrolidin-2-onyl)pyridineHCID 1969435181.1%

반응 조건

온도25 °C

반응 단계

5-(2-Hydroxy-2-methyl-3-butynyl)-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine (200 mg, 0.77 mmol) was dissolved in toluene (20 mL) and catalytic sodium hydride (5 mg) was added. The solution was heated until several milliliters of toluene-acetone mixture were removed by distillation. The mixture was cooled to 25° C. and water (10 mL) and ethyl acetate (20 mL) were added. The organic phase was separated and the aqueous layer extracted with ethyl acetate (2×20 mL) and the combined organic extracts were washed with brine (10 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by silica gel column chromatography with ethyl acetate as eluant to afford 5-ethynyl-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine as a solid (125 mg, 81%). M.p. 83°-84° C.; 1H NMR (CDCl3, 300 MHz): δ 8.69 (d, J=2 Hz, 1H), 8.46 (d, J=2 Hz, 1H), 7.62 (t, J=2 Hz, 1H), 4.57 (dd, J=7, 6 Hz, 1H), 3.28 (s, 1H), 2.70 (s, 3H), 2.45-2.65 (m, 3H), 1.88 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723477
출처 데이터셋uspto-grants-1998_03
ORD IDord-531fb851617d486f9d7f9ae162bfa0c1
출처 메모uspto-grants-1998_03