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HRID 386067作成日:2026年10月25日

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

https://huagongshe.com/reaction/386067

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethylsilylmethyl AzideHCID 150751—
反応物Sodium AscorbateHCID 23667548—
反応物2-Bromo-6-(1-fluoroprop-2-yn-1-yl)pyridineHCID 59525949—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒Sodium BicarbonateHCID 516892—
生成物2-Bromo-6-(fluoro{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methyl)pyridineHCID 59525895—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367706B2
出典データセットuspto-grants-2013_02
ORD IDord-91ced9ba13bd4ff0b33a986cbd7427cc
出典メモuspto-grants-2013_02