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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386067생성일: 2026년 10월 26일

Trimethylsilylmethyl Azide → 2-Bromo-6-(fluoro{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methyl)pyridine

https://huagongshe.com/reaction/386067

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilylmethyl AzideHCID 150751—
반응물Sodium AscorbateHCID 23667548—
반응물2-Bromo-6-(1-fluoroprop-2-yn-1-yl)pyridineHCID 59525949—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
용매Sodium BicarbonateHCID 516892—
생성물2-Bromo-6-(fluoro{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methyl)pyridineHCID 59525895—

반응 단계

2-Bromo-6-(1-fluoroprop-2-yn-1-yl)pyridine (520 mg, 2.43 mmol) and trimethylsilylmethyl azide (377 mg, 2.92 mmol) were combined in t-BuOH (5.0 mL) and water (3.0 mL). CuSO4.5H2O (30 mg, 0.12 mmol) in water (1.0 mL) was added, followed by sodium ascorbate (96 mg, 0.49 mmol) in water (1.0 mL). The reaction was stirred at room temperature overnight, diluted with saturated NaHCO3, and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated to a brown residue that was purified by flash chromatography (0-30% EtOAc/hexanes) to afford the title compound as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367706B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-91ced9ba13bd4ff0b33a986cbd7427cc
출처 메모uspto-grants-2013_02