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HRID 386059作成日:2026年10月26日

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

https://huagongshe.com/reaction/386059

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2-Bromo-6-ethynylpyridineHCID 12970532—
反応物Sodium AscorbateHCID 23667548—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒Sodium BicarbonateHCID 516892—
生成物2-Bromo-6-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}pyridineHCID 59525901—

反応手順

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.

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-2302a702b83c454e84c00efd094b899a
出典メモuspto-grants-2013_02