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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386059생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/386059

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilylmethyl AzideHCID 150751—
반응물2-Bromo-6-ethynylpyridineHCID 12970532—
반응물Sodium AscorbateHCID 23667548—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
용매Sodium BicarbonateHCID 516892—
생성물2-Bromo-6-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}pyridineHCID 59525901—

반응 단계

2-Bromo-6-ethynylpyridine (Example 465, Step 1) (350 mg, 1.92 mmol) and trimethylsilylmethyl azide (323 mg, 2.50 mmol) were combined in t-BuOH (4.0 mL) and water (3.0 mL). CuSO4.5H2O (24 mg, 0.096 mmol) in water (0.50 mL) was added, followed by sodium ascorbate (76 mg, 0.39 mmol) in water (0.50 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 yellow residue that was purified by flash chromatography (0-50% 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-2302a702b83c454e84c00efd094b899a
출처 메모uspto-grants-2013_02