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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 717249생성일: 2026년 10월 25일

Sodium Iodide → N'-[3-tert-butyl-1-(oxan-2-ylmethyl)pyrazol-5-yl]-N,N-dimethylmethanimidamide

https://huagongshe.com/reaction/717249

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium hydrideHCID 24758—
반응물2-(Bromomethyl)tetrahydro-2H-pyranHCID 141917—
반응물HCID 178484244HCID 178484244—
용매DimethylformamideHCID 6228—
생성물N'-[3-tert-butyl-1-(oxan-2-ylmethyl)pyrazol-5-yl]-N,N-dimethylmethanimidamideHCID 8744011355%

반응 조건

온도65 °C

반응 단계

To a solution of Example 63A (1.0 g, 5.2 mmol) in N,N-dimethylformamide (10 mL) were added sodium hydride (0.52 g, 12.9 mmol, 60% in mineral oil, Aldrich), 2-(bromomethyl)tetrahydro-2H-pyran (0.8 mL, 6.2 mmol) and sodium iodide (0.23 g, 1.5 mmol). After stirring at 65° C. for 16 h, the reaction mixture was cooled and quenched with saturated NaHCO3 (10 mL). The aqueous layer was extracted with ethyl acetate (3×20 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography using an Analogix® Intelliflash280™ (SiO2, 0-10% methanol in dichloromethane) to provide 0.82 g (55%) of the title compound. 1H NMR (501 MHz, chloroform-d) δ ppm 1.22-1.33 (m, 1H), 1.27 (s, 9H), 1.34-1.49 (m, 3H), 1.51-1.62 (m, 1H), 1.72-1.83 (m, 1H), 2.87 (s, 3H), 2.95 (s, 3H), 3.36-3.49 (m, 1H), 3.73-3.83 (m, 1H), 3.95 (dd, J=11.3, 3.0 Hz, 1H), 4.02 (dd, J=13.4, 7.7 Hz, 1H), 4.17 (dd, J=13.4, 5.8 Hz, 1H), 5.55 (s, 1H), 8.00 (s, 1H). MS (ESI+) m/z 293 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193713B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-573ca114e50e4708a4650b867a3a89da
출처 메모uspto-grants-2015_11